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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26174Generated: October 25, 2026

Triethylamine → 1-[beta-(2-Methyl-3-indolyl)propionyl]-4-benzyl-4-hydroxypiperidine

https://huagongshe.com/reaction/26174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant1H-Indole-3-propanoic acid, 2-methyl-HCID 97380—
Reactant4-Benzyl-4-piperidinolHCID 98152—
SolventChloroformHCID 6212—
Product1-[beta-(2-Methyl-3-indolyl)propionyl]-4-benzyl-4-hydroxypiperidineHCID 21324671—

Reaction Steps

To a stirred solution of 5.0 g of β-(2-methyl-3-indolyl)propionic acid and 2.5 g of triethylamine in 100 ml of chloroform was added dropwise 2.7 g of ethyl chloroformate at a temperature below 0° C. After the addition was complete, stirring was continued for additional 15 minutes and thereto was added 4.7 g of 4-benzyl-4-hydroxypiperidine in several portions. The reaction mixture was stirred for 4 hours at room temperature and allowed to stand overnight. The reaction product was washed thoroughly with water and concentrated to dryness. The residue was recrystallized from ethanol to give 1-[β-(2-methyl-3-indolyl)propionyl]-4-benzyl-4-hydroxypiperidine, melting at 117°-119° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04148796
Source datasetuspto-grants-1979_04
ORD IDord-3024e340990f494fa08720f195cbe64d
Source noteuspto-grants-1979_04