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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166363Generated: October 26, 2026

Tetrahydrofuran → 5(-4-Aminophenoxy)-4-methoxymethyl-beta-carboline-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/2166363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant5-(4-Nitrophenoxy)-4-methoxymethyl-beta-carboline-3-carboxylic acid ethyl esterHCID 13800058—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product5(-4-Aminophenoxy)-4-methoxymethyl-beta-carboline-3-carboxylic acid ethyl esterHCID 13800066—

Reaction Steps

15 g of 5-(4-nitrophenoxy)-4-methoxymethyl-beta-carboline-3-carboxylic acid ethyl ester is hydrogenated in 450 ml of methanol: tetrahydrofuran=1:1 with 7.5 g of palladium on carbon (10%) at room temperature under hydrogen normal pressure. After filtering and concentrating, it is recrystallized from ethanol and 10.8 g (77% of theory) of 5-(4-aminophenoxy)-4-methoxymethyl-beta-carboline-3-carboxylic acid ethyl ester of a melting point of 222°-224° C. is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04945090
Source datasetuspto-grants-1990_07
ORD IDord-38eb7e7c835c492295865c48e196f6c9
Source noteuspto-grants-1990_07