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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833595Generated: October 30, 2026

Methanol → 1-Methyl-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-acetic acid

https://huagongshe.com/reaction/1833595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium HydroxideHCID 14797—
Reactant1-Methyl-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-acetic acid ethyl esterHCID 53714247—
SolventWaterHCID 962—
Product1-Methyl-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-acetic acidHCID 10490571—

Reaction Steps

Hydrolysis of this ester to the title compound is effected as follows: The ester is dissolved in 230 ml. of methanol. To this is added 10 g. of KOH in 30 ml. of H2O and the solution is allowed to stand at room temperature overnight. The methanol is evaporated, water added and the solution washed with benzene. The aqueous phase is acidified with 6N HCl, and extracted with benzene. This organic phase is washed with water, dried over sodium sulfate and evaporated to dryness to give an oil, which is crystallized from benzen containing a trace of petroleum ether to afford the title compound, m.p. 150° - 152° C., νmaxCHCl3 3325 and 1705 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04066779
Source datasetuspto-grants-1978_01
ORD IDord-2901810befc24cbc92c929eac9b32b29
Source noteuspto-grants-1978_01