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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 653145생성일: 2026년 10월 24일

Benzyl Chloride → 1-Phenyl-3-(phenylmethoxy)-1H-indole-2-carboxylic acid methyl ester

https://huagongshe.com/ko/reaction/653145

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl ChlorideHCID 7503—
반응물Sodium hydrideHCID 24758—
반응물Methyl 3-hydroxy-1-phenyl-1H-indole-2-carboxylateHCID 54687160—
용매HexamethylphosphoramideHCID 12679—
생성물1-Phenyl-3-(phenylmethoxy)-1H-indole-2-carboxylic acid methyl esterHCID 1388582654%

반응 단계

A mixture of 1.2 g (0.025 mole) of 50% sodium hydride/mineral oil suspension in 20 ml of hexamethylphosphoramide under a nitrogen atmosphere was cooled in ice and treated over 15 minutes with a solution of 5.3 g (0.020 mole) of 3-hydroxy-1-phenyl-1H-indole-2-carboxlic acid methyl ester [P. Friedlander and K. Kurz, Chem. Ber., 55, 1597 (1922)] in 25 ml of hexamethylphosphoramide. The mixture was stirred in ice an additional one hour, 2.6 ml (2.9 g, 0.023 mole) of benzyl chloride was added in one portion, the ice bath was removed and stirring was continued for a total of 18 hours. The reaction mixture was added to 200 g of ice/water, stirred for one hour, and the precipitated product was filtered and washed with water. Recrystallization from aqueous methanol yielded 3.8 g (54% yield) of the ester product. An additional recrystallization as above yielded analytically pure ester, mp 117°-119° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04675332
출처 데이터셋uspto-grants-1987_06
ORD IDord-bcc7c97dd21844328ed5cb7d5875aa91
출처 메모uspto-grants-1987_06