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HRID 979711作成日:2026年10月27日

Dichloro(diethylamino)phosphine → Cyclohexyl(diethylamino)chlorophosphine

https://huagongshe.com/reaction/979711

反応式

関与物質

役割名称HCID仕込み量
反応物Dichloro(diethylamino)phosphineHCID 2733289—
反応物HCID 178478990HCID 178478990—
生成物Cyclohexyl(diethylamino)chlorophosphineHCID 436880257.5%

反応手順

U.S. Pat. No. 2,934,564 relates to compounds of the general formula R2PX wherein R represents an alkyl or aryl group and X represents chlorine, bromine or iodine. For example, the reaction of Me2NPCl2 (0.42 mole) with p-tolylmagnesium bromide (0.84 mole) produces dimethylamino-di-p-tolylphosphine. The isolated dimethylamino-di-p-tolylphosphine (31.88 mmoles) was treated with 1428 cc (63.75 mmoles) of anhydrous HCl yielding di-p-tolylchlorophosphine, which was purified by distillation. Similarly, Burg, et al. (J.A.C.S. 80, 1107-09, 1958) disclose the preparation of chlorodimethylphosphine from Me2NPCl2 and suggest the viability of a Grignard route to R2PR'-type phosphines. K. Issleib, et al. (Chem. Berichte 29, 2682-3008, 1959) have shown that Et2NPCl2 (Et=ethyl) and cyclohexylmagnesium chloride react in a 1:1.25 molar ratio to form diethylaminocyclohexylchlorophosphine in 57.5% yield. The authors suggest this reaction can be exploited to prepare unsymmetrical chlorophosphines of the type RR'PCl, but no mention is made of the possibility of further reaction to unsymmetrical tertiary phosphines of the type RR'R"P.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04668823
出典データセットuspto-grants-1987_05
ORD IDord-97bc99cfccb84eb7bff4ad4cbe27f189
出典メモuspto-grants-1987_05