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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575297Generated: October 31, 2026

Trifluoroacetic acid → Ethyl 9-bromo-4-methyl-4,5-dihydrobenzo[2,3]oxepino[4,5-d]thiazole-2-carboxylate

https://huagongshe.com/reaction/575297

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
ReactantEthyl 9-bromo-4-hydroxy-4-methyl-4,5-dihydrobenzo[2,3]oxepino[4,5-d]thiazole-2-carboxylateHCID 86693318—
SolventDichloromethaneHCID 6344—
ProductEthyl 9-bromo-4-methyl-4,5-dihydrobenzo[2,3]oxepino[4,5-d]thiazole-2-carboxylateHCID 8669332773.1%

Reaction Steps

TFA (891 mg, 7.88 mmol, 30.00 equiv) was added dropwise to a stirred solution of ethyl 9-bromo-4-hydroxy-4-methyl-4,5-dihydrobenzo[2,3]oxepino[4,5-d]thiazole-2-carboxylate (100 mg, 0.26 mmol, 1.00 equiv) and Et3SiH (454 mg, 3.90 mmol, 15.00 equiv) in dichloromethane (5 mL) at 0° C. After being stirred at room temperature overnight the reaction was quenched with 10 mL of saturated NaHCO3, extracted with 5×20 mL of ethyl acetate, dried over anhydrous sodium sulfate, and concentrated under vacuum. The residue was purified by a silica gel column with ethyl acetate/petroleum ether (1:15) to give 70 mg (73%) of the titled compound as a light yellow solid; LC-MS (ES, m/z) 368, 369 [M+11]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034866B2
Source datasetuspto-grants-2015_05
ORD IDord-bf7f068819d24b2f966bd7a9e3c8c43a
Source noteuspto-grants-2015_05