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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282860Generated: October 31, 2026

Dicyclohexylcarbodiimide → HCID 21533415, compound

https://huagongshe.com/reaction/1282860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2H-Thieno(2,3-c)(1)benzopyran-9-ol, 1,4-dihydro-7-(1,2-dimethylheptyl)-1,4,4-trimethyl-HCID 3043881—
Reactant4-(Piperidin-1-yl)butanoic acid hydrochlorideHCID 13172081—
SolventDichloromethaneHCID 6344—
ProductHCID 21533415HCID 21533415—

Reaction Steps

A combination of 2.4 g. (6.4 mmole) of 1,2-dihydro-9-hydroxy-7-(3-methyl-2-octyl)-1,4,4,-trimethyl-4H-thieno[2,3-c][1]benzopyran, 1.33 g. (6.4 mmole) of γ-piperidinobutyric acid hydrochloride, 1.40 g. (6.75 mmole) of dicyclohexylcarbodiimide and 125 ml. of methylene chloride was stirred at room temperature for 18 hours. The reaction mixture was cooled and the byproduct of dicyclohexylurea was removed by filtration. The methylene chloride was distilled off on a rotary evaporator to give a colorless, foamy residue, which was purified on 80 g. of magnesium silicate (60-100 mesh) using a graded methanol/chloroform solvent system. The fractions were monitored by thin layer chromatography, and the appropriate fractions were combined to give 1.23 g. (37%) of the desired material as a golden gum. The infrared and nuclear magnetic resonance spectra were in agreement with the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03972880
Source datasetuspto-grants-1976_08
ORD IDord-bfb38c029c95459eac970fec468e54cb
Source noteuspto-grants-1976_08