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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2118921생성일: 2026년 10월 25일

Pyridine → p-Nitrophenyl 5-benzyloxy-2,2-dimethyl-7-(1,1-dimethylheptyl)-3,4-dihydro-2H-benzopyran-4-carboxylate

https://huagongshe.com/reaction/2118921

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물4-Nitrophenyl trifluoroacetateHCID 69569—
반응물5-Benzyloxy-2,2-dimethyl-7-(1,1-dimethylheptyl)-3,4-dihydro-2H-benzopyran-4-carboxylic acidHCID 13364578—
용매PentaneHCID 8003—
생성물p-Nitrophenyl 5-benzyloxy-2,2-dimethyl-7-(1,1-dimethylheptyl)-3,4-dihydro-2H-benzopyran-4-carboxylateHCID 1336458080.2%

반응 단계

A mixture of 3.3 g (7.53 mmole) 5-benzyloxy-2,2-dimethyl-7-(1,1-dimethylheptyl)-3,4-dihydro-2H-benzopyran-4-carboxylic acid, 5.0 g (21.3 mmole) p-nitrophenyl trifluoroacetate and 100 ml dry pyridine, under nitrogen, is stirred at room temperature for three hours. The pyridine is evaporated in vacuo, ethyl ether is added to the residue and this is washed with 1N sodium hydroxide, water, 10% hydrochloric acid, brine, dried (MgSO4) and the solvent evaporated to obtain 4.5 g crude oil. This is taken up in pentane and cooled to obtain 3.38 g of crystals, m.p. 87°-87.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04680404
출처 데이터셋uspto-grants-1987_07
ORD IDord-c577b0a4d8c5405b8b1cdb10e169194f
출처 메모uspto-grants-1987_07