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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722306Generated: October 29, 2026

Bromine → 6-Bromo-7-(1,1-dimethylethyl)-2-(trifluoromethyl)-2h-1-benzopyran-3-carboxylic acid

https://huagongshe.com/reaction/722306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant7-(1,1-Dimethylethyl)-2-trifluoromethyl-2h-1-benzopyran-3-carboxylic acidHCID 9904406—
CatalystIronHCID 23925—
SolventChloroformHCID 6212—
Product6-Bromo-7-(1,1-dimethylethyl)-2-(trifluoromethyl)-2h-1-benzopyran-3-carboxylic acidHCID 21883679—

Reaction Steps

7-(1,1-Dimethylethyl-2-(trifluoromethyl)-2H-1-benzopyran-3-carboxylic acid (Example 12)(0.6 g, 2 mmol), chloroform (50 mL), iron filings (0.01 g, 0.2 mmol), and bromine (0.48 g, 3.00 mmol) were stirred at reflux for 16 h. The mixture was allowed to cool and was washed with brine (2×50 mL). After drying over MgSO4, the mixture was filtered, concentrated in vacuo, and the residue crystallized from ether-hexanes yielding the title compound as a white solid (0.5 g, 66%): mp 198.6–199.9° C. 1H NMR (acetone-d6/300 MHz) 7.85 (s, 1H), 7.72 (s, 1H), 7.13 (s, 1H), 5.83 (q, 1H, J=7.2 Hz), 1.5 (s, 9H). Anal. Calc'd for C15H14O3F3Br: C, 47.52; H, 3.72; N, 21.07. Found: C, 47.42; H, 3.68; N, 21.15.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138411B2
Source datasetuspto-grants-2006_11
ORD IDord-49fdd2dd0f584050b6c56ba7c407150b
Source noteuspto-grants-2006_11