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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267858Generated: October 26, 2026

1-Butanol → Dibutyl phenylphosphonite

https://huagongshe.com/reaction/267858

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ButanolHCID 263—
ReactantPhenyl phosphorus dichlorideHCID 12573—
ReactantButyl phenylphosphonochloridateHCID 15680480—
SolventDiethyl EtherHCID 3283—
ProductDibutyl phenylphosphoniteHCID 520472—

Reaction Steps

The starting material, butyl phenylphosphonochloridate, was prepared from dichlorophenylphosphine as follows: To a cold, stirred solution of 30.0 g of butanol and 41.4 g of trtiethylamine in about 300 ml of ethyl ether was added dropwise a solution of 34.6 g of dichlorophenylphosphine in about 200 ml of ethyl ether while the temperature was maintained below 0°. When addition was completed, the mixture was allowed to warm to room temperature. Stirring was continued overnight. The mixture was filtered, and the filtrate was concentrated under reduced pressure. The residual oil was distilled under reduced pressure to give 39.5 g of dibutyl phenylphosphonite, b.p. 120°-131°/ca 1.0 mm. Chlorine gas was bubbled into 38.5 g of dibutyl phenylphosphonite for about three hours. The mixture was warmed to 50° under aspirator vacuum to remove butyl chloride. The residual colorless oil was dissolved in 100 ml of benzene, washed with 1% sodium hydroxide and with water, dried over magnesium sulfate, and the dried solution concentrated under reduced pressure to give 30.6 g of pale yellow butyl phenylphosphonochloridate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03944666
Source datasetuspto-grants-1976_03
ORD IDord-8e6fa0ad96ee4a6ab34eaa8450ac22ed
Source noteuspto-grants-1976_03