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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257510Generated: October 28, 2026

Acetic Acid → HCID 54030218, compound

https://huagongshe.com/reaction/257510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1,4-ButanediolHCID 8064—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant(5-(3-Thienyl)tetrazol-1-yl)acetic acidHCID 3035658—
SolventDimethylformamideHCID 6228—
ProductHCID 54030218HCID 5403021860.3%

Reaction Steps

To a solution of 1 g (4.76 mM) of [5-(3-thienyl)tetrazol-1-yl] acetic acid and 514 mg (5.71 mM) of 1,4-butanediol in 10 ml of N,N-dimethylformamide was added 1.08 g (5.23 mM) of dicyclohexylcarbodiimide at room temperature. After the mixture was stirred at room temperature for 30 min, a small amount of acetic acid was added to the mixture and then was stirred for 30 min. The mixture was poured into ice-water. The precipitated crystal was filtered off and washed with water. The filtrate was extracted with ethyl acetate. The organic phase was washed with water, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The resultant residue was subjected to silica gel column chromatography (eluent: chloroform/ethyl alcohol=30/1) for separation and purification, to give 810 mg (yield 60.3%) of [5-(3-thienyl)tetrazol-1-yl] acetic acid 4-hydroxybutyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05262433
Source datasetuspto-grants-1993_11
ORD IDord-041007bf1efb4c338981c4f54b04519a
Source noteuspto-grants-1993_11