HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581620Generated: November 2, 2026
Trichlorosilane → Bis(3,5-di-t-butyl-4-methoxyphenyl)(2-bromophenyl)phosphine
https://huagongshe.com/reaction/1581620
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trichlorosilane | HCID 24811 | — |
| Reactant | Bis(3,5-di-t-butyl-4-methoxyphenyl)(2-bromophenyl)phosphine oxide | HCID 12115809 | — |
| Product | Bis(3,5-di-t-butyl-4-methoxyphenyl)(2-bromophenyl)phosphine | HCID 12115810 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06730629B2 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-34ef4b11040142829719db298173156a |
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| Source note | uspto-grants-2004_05 |
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