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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575293Generated: October 28, 2026

S,S-dimethylmethanesulfinyl iodide → HCID 86693323, compound

https://huagongshe.com/reaction/575293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantS,S-dimethylmethanesulfinyl iodideHCID 2723795—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantEthyl 9-bromo-4-oxo-4,5-dihydrobenzo[2,3]oxepino[4,5-d]thiazole-2-carboxylateHCID 86693324—
SolventDichloromethaneHCID 6344—
ProductHCID 86693323HCID 8669332348%

Reaction Steps

Into a 100-mL 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen was placed a solution of S,S-dimethylmethanesulfinyl iodide (1.15 g, 5.23 mmol, 1.60 equiv), t-BuOK (4 mL, 1.20 equiv) in dichloromethane (5 mL) at room temperature After 30 minutes a solution of ethyl 9-bromo-4-oxo-4,5-dihydrobenzo[2,3]oxepino[4,5-d]thiazole-2-carboxylate (1.2 g, 3.26 mmol, 1.00 equiv) in dichloromethane (10 mL) was added slowly. The resulting solution was stirred for 5 h at room temperature, quenched with water, extracted with dichloromethane, dried over anhydrous sodium sulfate, and concentrated under vacuum. The residue was purified by a silica gel column with ethyl acetate/petroleum ether (1:19) to give 600 mg (48%) of the titled compound as a off-white solid; LC-MS 382,384[M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034866B2
Source datasetuspto-grants-2015_05
ORD IDord-026c435b8af84c57b5123d4c49c51426
Source noteuspto-grants-2015_05