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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015609Generated: October 26, 2026

5-Fluoro-2-(trifluoromethyl)benzoyl chloride → Ethyl 2-{[5-fluoro-2-(trifluoromethyl)benzoyl]amino}-4,4,6,6-tetramethyl-4,6-dihydrothieno[2,3-c]furan-3-carboxylate

https://huagongshe.com/reaction/1015609

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Fluoro-2-(trifluoromethyl)benzoyl chlorideHCID 2737560—
Reactant2-Amino-4,4,6,6-tetramethyl-4,6-dihydrothieno[2,3-c]furan-3-carboxylic acid ethyl esterHCID 67300637—
ProductEthyl 2-{[5-fluoro-2-(trifluoromethyl)benzoyl]amino}-4,4,6,6-tetramethyl-4,6-dihydrothieno[2,3-c]furan-3-carboxylateHCID 24772746—

Reaction Steps

The title compound was prepared from the product of Example 18A and commercially available 5-fluoro-2-(trifluoromethyl)benzoyl chloride using the procedure described for Example 1B. 1H NMR (DMSO-d6, 300 MHz) δ 1.30 (t, J=7.1 Hz, 3H), 1.54 (s, 6H), 1.49 (s, 6H), 4.30 (q, J=7.1 Hz, 2H), 7.63-7.70 (m, 1H), 7.82 (dd, J=8.6, 2.5 Hz, 1H), 8.01 (dd, J=8.8, 5.1 Hz, 1H), 11.48 (br s, 1H). MS (ESI+) m/z 460 (M+H)+. Anal. calcd. for C21H21F4NO4S: C, 54.90; H, 4.61; N, 3.05. Found: C, 54.72; H, 4.68; N, 2.98.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985768B2
Source datasetuspto-grants-2011_07
ORD IDord-cbec66a23a184281bb5d000f7c33bd93
Source noteuspto-grants-2011_07