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HRID 484251作成日:2026年10月25日

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

https://huagongshe.com/reaction/484251

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl-1-propyl-1,3,4,9-tetrahydro-6-(phenylmethoxy)pyrano[3,4-b]indole-1-acetateHCID 19935728—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物Ethyl-1-propyl-1,3,4,9-tetrahydro-6-hydroxypyrano[3,4-b]indole-1-acetateHCID 1993574289.2%

反応手順

A suspension of the 6-benzyloxypyranoindole (5.4 g, 13.25 mmol) of Step A, and 10% Pd/C catalyst (600 mg) in ethanol (150 mL) is hydrogenated for 6 hours in a Parr shaker. Filtration of the catalyst and evaporation of the solvent affords the title compound (3.75 g, 89%) as a cream-colored foam 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-8374ba090dec41b98aeac5ce1bebb5e3
出典メモuspto-grants-1993_07