돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1353121생성일: 2026년 10월 27일

Phenyl cyanate → 4-Cyclopentyl-but-2-ynenitrile

https://huagongshe.com/reaction/1353121

반응식

참여 물질

역할이름HCID투입량
반응물Phenyl cyanateHCID 70740—
반응물(Prop-2-yn-1-yl)cyclopentaneHCID 521007—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
생성물4-Cyclopentyl-but-2-ynenitrileHCID 2110231747%

반응 조건

온도-78 °C

반응 단계

Prop-2-ynyl-cyclopentane (46.2 mmol) was dissolved in 100 mL of anhydrous Et2O under N2 and the reaction was cooled to −78° C. A 2.5 M solution of BuLi in hexanes (55.5 mmol) was added dropwise to the reaction over 30 minutes. The reaction was stirred for an additional 20 minutes and phenyl cyanate (55.5 mmol) was then added in solution with 20 mL of Et2O dropwise over 20 minutes. The resultant solution was allowed to slowly warm to rt and stir for 3 hours. The reaction material was then diluted in 200 mL of fresh Et2O and washed with three 100 mL portions of 1 N aqueous NaOH solution. The organics were then washed with 200 mL of brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified through flash chromatography on silica gel to give 4-cyclopentyl-but-2-ynenitrile (21.7 mmol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07220865B2
출처 데이터셋uspto-grants-2007_05
ORD IDord-58662001d63c48e79d3be55517eee19b
출처 메모uspto-grants-2007_05