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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371259Generated: October 31, 2026

Acetic Anhydride → HCID 67486354, compound

https://huagongshe.com/reaction/2371259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantBenzeneacetic acid, 4-(1,1-dimethylethyl)-HCID 118343—
ReactantMethyl 5-formylthiophene-2-carboxylateHCID 818924—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 67486354HCID 6748635467.2%

Reaction Conditions

Temperature120 °C

Reaction Steps

To (4-tert-butyl-phenyl)-acetic acid (1.15 g, 6.0 mmol) was added 5-formyl-thiophene-2-carboxylic acid methyl ester (1 g, 5.7 mmol), acetic anhydride (3.08 g, 30.2 mmol), and triethyl amine (574 mg, 5.7 mmol). The resulting mixture was stirred at 120° C. for 16 hours and cooled down. Water (1.9 ml) was added. The reaction mixture was heated up to 100° C. for 5 minutes in microwave and cooled down to 23° C. A mixture of acetic acid and water (2.5 ml:2.5 ml) was added. The resulting reaction mixture was stirred at 23° C. for 1 hour. The precipitate was filtered off, washed with 25% aqueous acetic acid, then water. The solid was dried under high vacuum to afford 5-[(E)-2-(4-tert-Butyl-phenyl)-2-carboxy-vinyl]-thiophene-2-carboxylic acid methyl ester as a brownish solid (1.32 g, 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710236B2
Source datasetuspto-grants-2014_04
ORD IDord-308e695ca1ce4f70bbf7d511557d7642
Source noteuspto-grants-2014_04