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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 842100생성일: 2026년 10월 27일

Triethylamine → 5-Chloro-2-(2-chlorophenyl)-7-(3-hydroxy-1-butynyl)-benzoxazole

https://huagongshe.com/reaction/842100

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-Butyn-2-olHCID 16239—
반응물7-Bromo-5-chloro-2-(2-chlorophenyl)-1,3-benzoxazoleHCID 4639254—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매TolueneHCID 1140—
생성물5-Chloro-2-(2-chlorophenyl)-7-(3-hydroxy-1-butynyl)-benzoxazoleHCID 4639255—

반응 단계

15.98 g (46.6 mmol) of 7-bromo-5-chloro-2-(2-chlorophenyl)-benzoxazole and 5 5.48 ml (69.9 mmol) of (±)-3-butyn-2-ol were heated for 6 h at 90-5° C. in 47 ml of toluene with 47 ml of triethylamine, 163.5 mg (233 μmol) of bis-triphenylphosphine-palladium(II)-dichloride and 8.9 mg (46.6 23 μmol) of copper(I) iodide. The reaction was filtered and the solid washed with toluene. The filtrate was evaporated in vacuo to dryness, the residue taken up in 150 ml of dichloromethane, extracted twice with 50 ml of 1 N HCl, dried with sodium sulfate, and filtered through 120 g of silica gel in a column. The title compound (11.11 g) was recovered as an off-white solid. A recrystallized sample from di-isopropyl ether had mp 129-31° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06372770B1
출처 데이터셋uspto-grants-2002_04
ORD IDord-67031ac3d51842e2b56c7159d7e2d5c1
출처 메모uspto-grants-2002_04