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HRID 484250作成日:2026年10月26日

Boron trifluoride etherate → Ethyl-1-propyl-1,3,4,9-tetrahydro-6-(phenylmethoxy)pyrano[3,4-b]indole-1-acetate

https://huagongshe.com/reaction/484250

反応式

関与物質

役割名称HCID仕込み量
反応物Boron trifluoride etherateHCID 8000—
反応物Ethyl 3-oxohexanoateHCID 238498—
反応物5-Benzyloxy-3-(2-hydroxyethyl)indoleHCID 744849—
溶媒DichloromethaneHCID 6344—
生成物Ethyl-1-propyl-1,3,4,9-tetrahydro-6-(phenylmethoxy)pyrano[3,4-b]indole-1-acetateHCID 1993572879.4%

反応手順

A solution of 5-benzyloxytryptophol (4.72 g, 17 mmol) and ethyl butyrylacetate (3.16 g, 20 mmol) in methylene chloride (75 ml) is treated dropwise with boron trifluoride etherate (3 mL) and stirred under nitrogen at room temperature overnight. The reaction mixture is diluted with methylene chloride (250 mL) and sequentially washed with 5% aqueous sodium bicarbonate (2×100 mL) and water (2×50 mL). The organic phase is dried (MgSO4), filtered, and evaporated to afford 7.0 g of a crude dark oil. Purification by flash column chromatography (ethyl acetate:hexane, 1:9 eluent) on silica gel (50:1 ratio, 230-400 mesh) affords the title compound (5.5 g, 79%) as a slightly amber oil homogeneous by TLC.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05229516
出典データセットuspto-grants-1993_07
ORD IDord-ec31bd7fc93543aeb39e2d420fc1594d
出典メモuspto-grants-1993_07