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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248959Generated: October 27, 2026

Triethylamine → alpha-(4-Methoxybenzoyl)-alpha-[1-(4-carboxyphenyl)-5-tetrazolylthio]-2-chloro-5-dodecyloxycarbonylacetanilide

https://huagongshe.com/reaction/1248959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 86741145HCID 86741145—
ReactantHCID 178524450HCID 178524450—
SolventChloroformHCID 6212—
Productalpha-(4-Methoxybenzoyl)-alpha-[1-(4-carboxyphenyl)-5-tetrazolylthio]-2-chloro-5-dodecyloxycarbonylacetanilideHCID 8674114693.3%

Reaction Steps

33 g of α-chloro-α-(4-methoxybenzoyl)-2-chloro-5-dodecyloxycarbonylacetanilide and 16 g of 1-(4-carboxyphenyl)-5-mercaptotetrazole were dispersed in 200 ml of chloroform to which was added dropwise 10 ml of triethylamine at room temperature over a period of about 30 minutes. After stirring for 3 hours the chloroform solution was washed with water and concentrated under reduced pressure. The residue was recrystallized from methanol to obtain 41.2 g of α-(4-methoxybenzoyl)-α-[1-(4-carboxyphenyl)-5-tetrazolylthio]-2-chloro-5-dodecyloxycarbonylacetanilide. Yield: 93%. Melting Point: 172° to 174° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04628024
Source datasetuspto-grants-1986_12
ORD IDord-6fcad6eccd0d40518c24aeffb2ff0aa7
Source noteuspto-grants-1986_12