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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776657Generated: November 3, 2026

2-Thiophenecarboxylic acid → HCID 86679604, compound

https://huagongshe.com/reaction/1776657

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiophenecarboxylic acidHCID 10700—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl bromoacetateHCID 79177—
SolventAcetoneHCID 180—
ProductHCID 86679604HCID 86679604100%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of thiophene-2-carboxylic acid (500 mg, 3.90 mmol) in acetone (20 ml), K2CO3 (593 mg, 4.29 mmol) was added, and mixture was stirred for 5 minutes, then KI (64.8 mg, 0.390 mmol) was added, followed by dropwise addition of tert-butyl 2-bromoacetate (0.634 ml, 4.29 mmol). The mixture was heated at 50° C. overnight. The solid residue was filtered out and washed with DCM; the solvent was evaporated and 2-tert-butoxy-2-oxoethyl thiophene-2-carboxylate was obtained as a clear oil (945 mg, 3.90 mmol, 100% yield, MS/ESI+ 264.9 [MNa]+) and used in the following reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09265768B2
Source datasetuspto-grants-2016_02
ORD IDord-84e45c5ea85d4c33838dc4bdd875b744
Source noteuspto-grants-2016_02