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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 638910생성일: 2026년 10월 27일

3-Allyl-4-allyloxy-5-methoxybenzoic acid → 9-Methoxy-2,5-dihydrobenzo[b]oxepine-7-carboxylic acid

https://huagongshe.com/reaction/638910

반응식

참여 물질

역할이름HCID투입량
반응물3-Allyl-4-allyloxy-5-methoxybenzoic acidHCID 68685212—
촉매Benzylidenebis(tricyclohexylphosphine)dichlororutheniumHCID 11967259—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물9-Methoxy-2,5-dihydrobenzo[b]oxepine-7-carboxylic acidHCID 68688134100.3%

반응 단계

To a stirred solution of 3-allyl-4-allyloxy-5-methoxybenzoic acid (200 mg, 0.81 mmol) in CH2Cl2 (20 mL) at room temperature was added benzylidene-bis-(tricyclohexylphosphine)dichlororuthenium (Grubb's catalyst, 35 mg, 0.04 mmol, 0.05 eq.). After stirring for 2 h the reaction was diluted with EtOAc (150 mL) then extracted with 2.0 N NaOH (100 mL). Aqueous layer was treated with brine (100 mL) then acidified to pH 5 using 1.0 N HCl. The aqueous layer was then extracted with EtOAc (2×200 mL). The organic layer was dried over MgSO4 and then concentrated in vacuo to afford 9-methoxy-2,5-dihydrobenzo[b]oxepine-7-carboxylic acid (179 mg, 100%) which was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07691843B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-b4a45f6ff79c48638c49dc1b87b003f3
출처 메모uspto-grants-2010_04