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HRID 556473作成日:2026年10月26日

Ethyl 6-methoxy-1H-indole-2-carboxylate → Rac-6-methoxy-2,3-dihydro-1h-indole-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/556473

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 6-methoxy-1H-indole-2-carboxylateHCID 612959—
反応物Sodium cyanoborohydrideHCID 5003444—
溶媒Trifluoroacetic acidHCID 6422—
生成物Rac-6-methoxy-2,3-dihydro-1h-indole-2-carboxylic acid ethyl esterHCID 5747905775.3%

反応手順

Sodium cyanoborohydride (750 mg, 12 mmol) (Aldrich) was added in small portions to a mixture of 6-Methoxy-1H-indole-2-carboxylic acid ethyl ester (500 mg, 2.4 mmol) (Aldrich) in TFA (10 mL), which was cooled in ice-water bath, at such a rate that gas evolution was not too vigorous. When the addition was complete, the mixture was allowed to warm to room temperature and stirred for 2.5 hr. The resulting mixture was concentrated in vacuo and the residue was dissolved in DCM. The organic layer was washed with Na2CO3 solution, dried with Na2SO4, and concentrated to give 400 mg rac-6-Methoxy-2,3-dihydro-1H-indole-2-carboxylic acid ethyl ester. MS: [M+H]+=222

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08058269B2
出典データセットuspto-grants-2011_11
ORD IDord-3b507d3ac117459fb37570dde41f7ff5
出典メモuspto-grants-2011_11