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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Diethyl 2-[bis(3,5-di-t-butyl-4-methoxyphenyl)phosphino]phenylphosphonite | HCID 12115811 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Product | 2-(Bis(3,5-di(tert-butyl)-4-methoxyphenyl)phosphino)phenylphosphine | HCID 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
| 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-103a353f76d94c2ca70154936db84e33 |
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| Source note | uspto-grants-2004_05 |
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