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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979710Generated: October 29, 2026

Hydrochloric Acid → BIS(4-METHYLPHENYL)CHLOROPHOSPHINE

https://huagongshe.com/reaction/979710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 20200975HCID 20200975—
ProductBIS(4-METHYLPHENYL)CHLOROPHOSPHINEHCID 4188608—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04668823
Source datasetuspto-grants-1987_05
ORD IDord-72acc3bf2711424fa721c7a47b6817ff
Source noteuspto-grants-1987_05