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HRID 2078494생성일: 2026년 10월 27일

Triphenylphosphine → 1-Bromo-5-trimethylsilylpent-2-en-4-yne

https://huagongshe.com/reaction/2078494

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물N-bromobutanimideHCID 67184—
반응물5-(Trimethylsilyl)pent-2-EN-4-YN-1-OLHCID 10975713—
용매DichloromethaneHCID 6344—
생성물1-Bromo-5-trimethylsilylpent-2-en-4-yneHCID 5728080389%

반응 단계

N-Bromosuccinimide (85.3 g, 0.48 mol) was added in portions to a nearly homogeneous solution of triphenylphosphine (128.2 g, 0.49 mol) and 2E-5-trimethylsilylpent-2-en-4-yn-1-ol (72.5 g, 0.47 mol) in dichloromethane (600 mL) under nitrogen and cooled in a dry ice/2-propanol bath to an initial temperature of below −20° C. The internal temperature of the reaction mixture was maintained at −10° C. to 0° C. throughout the addition by adjusting the rate of addition. The bath was allowed to warm to ambient temperature. After 2 hours, the reaction was complete. The reaction mixture was concentrated under vacuum to a thick paste and the residue was triturated with hexane (250 mL). The suspension was filtered and the solids and silica gel were rinsed with hexane (10×150 mL). The filtrate was concentrated under vacuum (30° C./60 mtorr) to obtain 44 g (89% yield) of 1-bromo-5-trimethylsilylpent-2-en-4-yne, a compound of formula (P), as a pale yellow oil: 1H-NMR (300 mHz, CDCl3) δ 0.19 (s, 9H), 3.95 (d, 2H), 5.75 (d, 1H), 6.31 (dt, 1H) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07928255B2
출처 데이터셋uspto-grants-2011_04
ORD IDord-e358607c1d37452c8d81a39f9efa0785
출처 메모uspto-grants-2011_04