Alcohol mass spectra

Saturated aliphatic alcohols. Mass spectra have been given for methanol (Unknown 1.3), 2-propanol (Figure 6.3), 3-methyl-3-hexanol (Figure 4.2), 4-octanol (Unknown 4.19), 1-dodecanol (Figure 3.8), 1-hexadecanol (Unknown 5.8), glycerol (Unknown 8.11), 2-aminoethanol (Unknown 4.2), and a-(aminomethyl-l-ethyl)-benzyl alcohol (Figure 4.5). 

Dakin oxidation 419, 420 Dakin rearrangement 799, 800 Dehalogenation 1098-1100 Dehydrodiconiferyl alcohol, mass spectrum of... 

The most intense peaks in the mass spectrum of an alcohol correspond to the ton formed according to carbon-carbon cleavage of the type shown ... 

Mass Spectrometry Ethers like alcohols lose an alkyl radical from their molecular ion to give an oxygen stabilized cation Thus m/z 73 and m/z 87 are both more abun dant than the molecular ion m the mass spectrum of sec butyl ethyl ether... 

Mass Spectrometry The molecular- ion peak is usually quite small in the mass spectrum of an alcohol. A peak conesponding to loss of water is often evident. Alcohols also fragment readily by a pathway in which the rnoleculai- ion loses an alkyl group from the... 

The mass spectra of alcohols often completely lack a peak corresponding to the parent ion. This is due to extremely rapid loss of neutral fragments following initial ionization. For example, the mass spectrum of 2-methyl-2-butanol lacks a parent peak and contains strong peaks at M-15 (loss of CH3O and M-18 (loss of H2O). 

The first 125 ml of eluent contained no alkaloids, but the next 150 ml yielded a crude alkaloid (115 mg). This alkaloid was crystallize from alcohol to yield 59 mg of slightly colored plates, mp 113-115. Subsequent recrystallizations raised the melting point to 121-122° (pale-yellow plates). The mass spectrum exhibited a parent ion at m/z 353. The UV spectrum showed maxima at 260 and 332 nm,... 

Basic hydrolysis of 6 afforded alcohol 19 and methyl veratrate. The H-NMR spectrum of 19 (Table II) revealed the presence of one methylenedioxy, one N-methyl, and two methoxyl groups. The mass spectrum (Table IV) exhibited the most abundant and significant ion peak at m/z 229 indicative of metaphanine-type cleavage. Treatment of an aqueous THF solution of stephavanine (18) with excess sodium hydride and methyl iodide gave N.O-dimethylstephine, a compound identical to alcohol 19. Thus, the structure of the new alkaloid 6 was established by chemical correlation with stephavanine (79). 

Figure 15. (a) Mass spectrum of alcohol clusters about Li+. Data taken at T = 150 K and (b) same as (a) but with an expanded intensity scale An = Li+(CH30H) Bn = Li+(CH30H) (H20). Taken with permission from ref. 106. 

Fig. 3. (Top left) Chemical methods used to depolymerize the polyesters. (Top right) Thin-layer and gas-liquid chromatograms (as trimethylsilyl derivatives) of the monomer mixture obtained from the cutin of peach fruits by LiAlD4 treatment. In the thin-layer chromatogram the five major spots are, from the bottom, C18 tetraol, C16 triol, and C18 triol (unresolved), diols, and primary alcohol. Nx = C16 alcohol N2= C18 alcohol Mj = C16 diol M2 = C18 diol D = C16 triol D2 and D3 = unsaturated and saturated C18 triol, respectively, T4 and T2, unsaturated and saturated C18 tetraol, respectively. (Bottom) Mass spectrum of component D3 in the gas chromatogram. BSA = bis-N,O-trimethylsilyl acetamide...

Detailed examination of another madder preparation proved that the sample can be premordanted with alum. [ 19] After hydrolysis performed with hydrochloric acid and extraction with M-amyl alcohol, only four colourants are found alizarin, purpurin, and probably lucidin and ruberythric acid. Additionally, signals at m/z 525 and 539 are observed in the mass spectrum. Analysis of the preparation by inductively coupled plasma mass spectrometry (ICP MS) shows that aluminium and calcium are the main inorganic components of the sample. This is why it was suggested that the signal at m/z 539 can be attributed to the complex of aluminium with alizarin, and the second one, observed at m/z 525, to an aluminium-calcium cluster. 

A systematic investigation of the free amino acids of the Leguminosae led to the isolation of a novel ninhydrin-positive compound from the leaves of Derris elliptica Benth. (Papilionidae) (93). This substance was analyzed as C6H,3N04 (microanalysis and high resolution mass spectrometry) and was shown to be an amino alcohol. The absence of a carbonyl in the 1R, the loss of 31 mass units in the mass spectrum, and a positive periodate cleavage reaction were best embodied into a dihydroxydihydroxymethylpyrrolidine structure. The relative simplicity of the NMR spectra (three peaks in the 13C spectrum four spin-system in the H spectrum) pointed out a symmetrical structure. Inasmuch as the material was optically active ([a]D 56.4, c = 7, H20), meso structures were ruled out, and the 2R, 3R, 4R, 5R relative configuration was retained (93). This structure (53) was further confirmed by an X-ray determination (94). 

For some molecules no molecular ion is visible in the mass spectrum as in ter. butyl alcohol, (CH3)3 COH in which the heaviest ion occurs at mass 59. corresponding to M+ - CH3 (74 - 15). So in such cases care must be taken in the interpretation of the spectra. 

Example The El mass spectra of 1-hexanol, Mj = 102, and 1-hexene, Mr = 84, show close similarity because the molecular ion peak is absent in the mass spectrum of hexanol (Fig. 6.40). However, a more careful examination of the hexanol spectrum reveals peaks at m/z 18, 19, 31, and 45 that are absent in the hexene spectrum. These are due to H20, HsO and to oxonium ions (H2C=OH and H3CCH=0H in this case) which are reliable indicators of aliphatic alcohols and ethers (Table 6.8). 

Figure 4. Mass Spectrum of Ferulate Ester of Behenyl Alcohol...

During the workup of the o-xylene oxidation run, a strong lachrymator made its presence felt. This was probably a-bromo-o-xylene, although it was not detected in the low voltage mass spectrum. We suspected that a strong peak at mass 104, undoubtedly caused chiefly by a fragment ion derived from o-methylbenzyl alcohol by loss of H20 (I), might also contain a contribution from benzocyclobutene from the interaction of a-bromo-o-xylene with the indium tube used to introduce samples into the spectrometer. To test this possibility, benzyl bromide and a-bromo-o-xylene were run separately under the same conditions. 

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