Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979709Generated: October 30, 2026

Iodine → HCID 20200975, compound

https://huagongshe.com/reaction/979709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantBromineHCID 24408—
ReactantChlorineHCID 24526—
ReactantN,N-Dimethylphosphoramidous dichlorideHCID 136483—
ReactantHCID 178418370HCID 178418370—
ProductHCID 20200975HCID 20200975—

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-e3f11074a7b14636ac226f899e8ba7b0
Source noteuspto-grants-1987_05