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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051608Generated: October 27, 2026

Methyl chloroformate → Benzoic Acid

https://huagongshe.com/reaction/2051608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantSodium AcetateHCID 517045—
ReactantHCID 20379237HCID 20379237—
Reactant4-(2-Aminoethyl)-benzoic acid sodiumHCID 70590830—
SolventAcetoneHCID 180—
SolventTriethylamineHCID 8471—
ProductBenzoic AcidHCID 243—

Reaction Steps

2.8 g of triethylamine and 2.6 g of chloroformic acid methyl ester are added, while stirring and cooling with ice, to 6.1 g of 2-butoxy-5-chloro-6-methyl-nicotinic acid (melting point 95°-97° C., prepared by chlorinating 2-butoxy-6-methyl-nicotinic acid in dilute glacial acetic acid) in 75 ml of acetone. The mixture is stirred for a further 15 minutes and then added, while stirring, to 25 ml of a 1-molar solution of 4-(2-amino-ethyl)-benzoic acid-sodium, additionally containing 0.025 mol of sodium acetate and to which 25 ml of acetone has been added. Stirring of the mixture is continued for 2 hours at room temperature, the acetone is removed under reduced pressure, the remaining aqueous solution is acidified, the precipitated reaction product is filtered off with suction, reprecipitated from ammonia and recrystallized from dilute methanol or ethyl acetate. The 4-(2-<2-butoxy-5-chloro-6-methyl-nicotinamido>-ethyl)-benzoic acid obtained melts at 148°-150° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04181658
Source datasetuspto-grants-1980_01
ORD IDord-cce071f07ec347b98dd8c54d8dd9d893
Source noteuspto-grants-1980_01