돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 324166생성일: 2026년 10월 23일

Triethylamine → HCID 15405387, 화합물

https://huagongshe.com/ko/reaction/324166

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Cyanogen BromideHCID 10476—
반응물ChavicolHCID 68148—
용매DichloromethaneHCID 6344—
생성물HCID 15405387HCID 1540538766%

반응 단계

To a solution of 2.142 g (15.96 mmol) of 4-(2-propenyl)phenol (prepared as in Example 1) in 15 mL of methylene chloride was added 2.351 g (22.19 mmol) of cyanogen bromide (Aldrich). The mixture was cooled in an ice-salt bath and 3 mL (22 mmol) of triethylamine was added dropwise with stirring. The mixture was stirred for an additional 15 minutes. The solvent was removed under vacuum and the mixture was transferred to a separatory funnel with 25 mL of water and 75 mL of petroleum ether (30-60° C. boiling range). The aqueous and organic layers were separated. The organic layer was washed with three 50 mL portions 6 N hydrochloric and one 50 mL portion of saturated sodium bicarbonate, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under vacuum to yield 1.668 g (66%) of crude 1-cyanato-4-(2-propenyl)benzene. The product was distilled to yield 1.307 g (51%) of 1-cyanato-4-(2-propenyl)benzene. The structure of the product was verified by IR and NMR spectroscopy. The product can be further purified by passing the product through a silica gel column using 1% toluene in petroleum ether as the solvent system.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06217943B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-efaf547bfc2f47fb8793d8467ac25d52
출처 메모uspto-grants-2001_04