Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67226Generated: October 26, 2026

Triethanolamine → 1-[2-(Ethoxycarbonyl)aminophenyl]-1'-methylspiro[indoline-3,4'-piperidine]

https://huagongshe.com/reaction/67226

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethanolamineHCID 7618—
ReactantEthyl chloroformateHCID 10928—
Reactant1-(2-Aminophenyl)-1'-methylspiro[indoline-3,4'-piperidine]dihydrochlorideHCID 12801598—
SolventChloroformHCID 6212—
Product1-[2-(Ethoxycarbonyl)aminophenyl]-1'-methylspiro[indoline-3,4'-piperidine]HCID 12801608—

Reaction Steps

A slurry of 10.36 g of 1-(2-aminophenyl)-1'-methylspiro[indoline-3,4'-piperidine]dihydrochloride of Example 1b in 60 ml of chloroform is treated portionwise with 12.3 ml of triethanolamine. The resulting mixture is cooled in an ice bath and treated dropwise over 40 minutes with a solution of 2.7 ml of ethyl chloroformate in 20 ml of chloroform. After stirring at room temperature for 1 hour, an additional 3.0 ml of ethyl chloroformate is added and the mixture is permitted to stand 16 hours. The product is washed thrice with water, brine, dried over anhydrous sodium sulfate, concentrated and pumped on under high vacuum to give a crude carbamate. Chromatography on silica gel (100 g) using ether-methylene chloride affords an oil. The material crystallizes on prolonged standing to yield 1-[2-(ethoxycarbonyl)aminophenyl]-1'-methylspiro[indoline-3,4'-piperidine], mp 99.5°-101.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04345081
Source datasetuspto-grants-1982_08
ORD IDord-17131cdffb2e493e80b8b86d526385a9
Source noteuspto-grants-1982_08