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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166368Generated: November 1, 2026

5-Phenoxy-4-methoxymethyl-beta-carboline-3-carboxylic acid → 5-Phenoxy-4-methoxymethyl-beta-carboline-3-carboxylic acid t-butyl ester

https://huagongshe.com/reaction/2166368

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Phenoxy-4-methoxymethyl-beta-carboline-3-carboxylic acidHCID 23039441—
SolventWaterHCID 962—
Product5-Phenoxy-4-methoxymethyl-beta-carboline-3-carboxylic acid t-butyl esterHCID 1380011574.6%

Reaction Steps

300 mg of 5-phenoxy-4-methoxymethyl-beta-carboline-3-carboxylic acid is heated with 2 ml of aminal ester for 3 hours to 120° C., whereby a solution is produced. After diluting with water, it is extracted with ethyl acetate. The organic phase is dreid, filtered, concentrated and chromatographed over silica gel with acetone:hexane=1:1 as eluant. 130 mg of 5-phenoxy-4-methoxymethyl-beta-carboline-3-carboxylic acid t-butyl ester with a decomposition point of 150° C. is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04945090
Source datasetuspto-grants-1990_07
ORD IDord-5a4bcacb772c42b1b6ec568f0c17e695
Source noteuspto-grants-1990_07