HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168635Generated: October 27, 2026
Chlorotrimethylsilane → 2-[Di(1-naphthyl)phosphino]phenylphosphine
https://huagongshe.com/reaction/1168635
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Diethyl 2-[di(1-naphthyl)phosphino]phenylphosphonite | HCID 11488538 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Product | 2-[Di(1-naphthyl)phosphino]phenylphosphine | HCID 11176875 | — |
Reaction Steps
For example, 2-bromophenol (4) is reacted with trifluoromethanesulfonic anhydride to form 2-(trifluoromethanesulfonyl)oxy-bromobenzene (5), which is then reacted with di(1-naphthyl)phosphine in the presence of a palladium complex catalyst to obtain (2-bromophenyl)[di(1-naphthyl)]phosphine (6). Next, the compound (6) is reacted with diethyl chlorophosphite in the presence of n-butyllithium to obtain diethyl 2-[di(1-naphthyl)phosphino]phenylphosphonite (7). Then, the compound (7) is reduced with lithium aluminum hydride in the presence of chlorotrimethylsilane to form [2-[di(1-naphthyl)phosphino]phenylphosphine (8). Thereafter, in the presence of n-butyllithium, the compound is reacted with dimesylate of (2R,5R)-2,5-hexanediol producible, for example, according to the method described in a literature (Tetrahedron: Asymmetry, 1991, 2, 569), whereby the aimed (S,S)-Me-UCAP-(1-Nap) (3) can be produced in a high efficiency.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06624320B2 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-e3595c231a514519b9c7c626a15ad924 |
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| Source note | uspto-grants-2003_09 |
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