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HRID 915551생성일: 2026년 10월 27일

3-Chloro-2-chloromethyl-1-propene → Di(tert-butyl)[2-(chloromethyl)-2-propenyl]phosphine

https://huagongshe.com/reaction/915551

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참여 물질

역할이름HCID투입량
반응물3-Chloro-2-chloromethyl-1-propeneHCID 15859—
반응물Phosphine, bis(1,1-dimethylethyl)-HCID 136643—
반응물9-(2-{[Di(tert-butyl)phosphino]methyl}-2-propenyl)-9-phosphabicyclo[3.3.1]nonaneHCID 58958856—
용매AcetonitrileHCID 6342—
생성물Di(tert-butyl)[2-(chloromethyl)-2-propenyl]phosphineHCID 8676054240%

반응 조건

온도60 °C

반응 단계

FIG. 1: 9-(2-{[di(tert-butyl)phosphino]methyl}-2-propenyl)-9-phosphabicyclo[3.3.1]nonane A mixture of di-tert-butylphoshine (5 g, 34.1 mmol) and 3-chloro-2-chloromethyl-1-propene (14.04 g, 69 mmol) was dissolved in degassed acetonitrile (70 ml) and heated to 60° C. for 16 hours. The solvent was removed in vacuo and the product was suspended in hexane (50 ml). After filtration the product was washed with hexane (2 times 40 ml). The white solid salt was neutralized in a mixture of toluene (50 ml) and water (30 ml) with HNEt2 (5 ml) under reflux conditions. The toluene layer was separated, washed with water (2 times 30 ml) and removed in vacuo, to yield 3.14 g (40%) of di(tert-butyl)[2-(chloromethyl)-2-propenyl]phosphine. The product could be characterized by showing a distinct resonance signals in 31P NMR at δ=+21.7 ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07265242B2
출처 데이터셋uspto-grants-2007_09
ORD IDord-e9d084c5866543be9da476cbeaabc1c6
출처 메모uspto-grants-2007_09