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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581622Generated: November 1, 2026

Chlorotrimethylsilane → 2-(Bis(3,5-di(tert-butyl)-4-methoxyphenyl)phosphino)phenylphosphine

https://huagongshe.com/reaction/1581622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantDiethyl 2-[bis(3,5-di-t-butyl-4-methoxyphenyl)phosphino]phenylphosphoniteHCID 12115811—
ReactantAluminium lithium hydrideHCID 21226445—
Product2-(Bis(3,5-di(tert-butyl)-4-methoxyphenyl)phosphino)phenylphosphineHCID 11376652—

Reaction Steps

For example, referring to the reaction sequence shown below, 2-bromophenol (4) is reacted with trifluoromethanesulfonic anhydride to form 2-(trifluoromethanesulfonyl)oxy-bromobenzene (5), which is then reacted with bis(3,5-di-t-butyl-4-methoxyphenyl)phosphine oxide in the presence of a palladium complex catalyst to obtain bis(3,5-di-t-butyl-4-methoxyphenyl)(2-bromophenyl)phosphine oxide (6). Next, the compound (6) is reduced with trichlorosilane in the presence of N,N′-dimethylaniline to obtain bis(3,5-di-t-butyl-4-methoxyphenyl)(2-bromophenyl)phosphine (7). The compound (7) is reacted with diethyl chlorophosphonite in the presence of n-butyllithium to obtain diethyl 2-[bis(3,5-di-t-butyl-4-methoxyphenyl)phosphino]phenylphosphonite (8). Then, the compound (8) is reduced with lithium aluminum hydride in the presence of trimethylsilyl chloride to form 2-[bis(3,5-di-t-butyl-4-methoxyphenyl)phosphino]phenylphosphine (9). Thereafter, in the presence of n-butyllithium, the compound (9) is reacted with dimesylate of (2R,5R)-2,5-hexanediol, which is producible, for example, according to the method described in the literature (Tetrahedron: Asymmetry, 1991, 2, 569), whereby the aimed (S,S)-Me-UCAP-DTBM (3) can be produced in a high efficiency.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06730629B2
Source datasetuspto-grants-2004_05
ORD IDord-103a353f76d94c2ca70154936db84e33
Source noteuspto-grants-2004_05