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Girard’s reagents

Girard s reagents Quaternary ammonium salts of the type Me3NCH2CONHNH2 X which form water-soluble compounds with aldehydes and ketones, and are therefore separable from other neutral compounds the aldehyde or ketone may be subsequently regenerated after separation. [Pg.190]

Girard s reagent T is carbohydrazidomethyltrimethylammonium chloride (I) and is prepared by the reaction of the quaternary ammonium salt formed from ethyl chloroacetate and trimethylamine with hydrazine hydrate in alco-hoUc solution ... [Pg.976]

Girard s reagent P , C5H5NCH2C0NHNH2 C1. In a 1-htre threenecked flask, equipped as in the previous preparation, place 200 ml. of absolute ethyl alcohol, 63 g. (64 -5 ml.) of pure anhydrous pyridine and 98 - 5 g. (84 5 ml.) of ethyl chloroacetate. Heat the mixture under reflux for 2-3 hours until the formation of the quaternary salt is complete acidify a small test-portion with dilute sulphuric acid it should dissolve completely and no odour of ethyl chloroacetate should be apparent. Cool the mixture in ice and salt. Replace the thermometer by a dropping funnel, and add a solution of 40 g. of 100 per cent, hydrazine hydrate in 60 ml. of absolute ethanol all at once. A vigorous exothermic reaction soon develops and is accompanied by vigorous effervescence. The pro duct separates almost immediately. When cold, filter with suction, wash... [Pg.977]

Steroid ketones Apply the sample solution followed by Girard s reagent (0 1% tnmethylacetyl hydrazide in 10% acetic acid) and allow to react for 15 h in an atmosphere of acetic acid Then dry at 80 °C for 10 mm and after cooling chromatograph the hydrazones that have been formed [81]... [Pg.72]

Other hydrazine derivatives frequently used to prepare the corresponding hydrazone are semicarbazide (NH2NHCONH2), in which case the hydrazone is called a semicarbazone, and Girard s reagents Tand P, in which case the hydrazone... [Pg.1193]

For a study of the mechanism with Girard s reagent T, see Stachissini, A.S. do Amaral, L. [Pg.1262]

Further methods of isolation were later developed [20-23]. The isolation was mostly effected by the use of Girard s reagent T to separate the keto steroids from the non-keto compounds, and each fraction was then separated by adsorption or partition chromatography. [Pg.173]


See other pages where Girard’s reagents is mentioned: [Pg.976]    [Pg.976]    [Pg.977]    [Pg.977]    [Pg.978]    [Pg.1191]    [Pg.10]    [Pg.96]    [Pg.1193]    [Pg.1193]    [Pg.1193]    [Pg.2390]    [Pg.486]    [Pg.487]    [Pg.730]    [Pg.976]    [Pg.976]    [Pg.977]    [Pg.977]    [Pg.978]    [Pg.1197]    [Pg.288]    [Pg.292]    [Pg.181]    [Pg.905]    [Pg.905]    [Pg.905]    [Pg.976]   
See also in sourсe #XX -- [ Pg.72 ]

See also in sourсe #XX -- [ Pg.72 ]

See also in sourсe #XX -- [ Pg.10 , Pg.18 ]

See also in sourсe #XX -- [ Pg.72 ]

See also in sourсe #XX -- [ Pg.10 , Pg.18 ]

See also in sourсe #XX -- [ Pg.136 ]

See also in sourсe #XX -- [ Pg.805 ]

See also in sourсe #XX -- [ Pg.139 ]




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Girard Reagent

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