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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506511Generated: October 31, 2026

Iodine → Methyl 4-iodo-3-phenylisothiazole-5-carboxylate

https://huagongshe.com/reaction/1506511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPentyl nitriteHCID 10026—
ReactantMethyl 4-amino-3-phenyl-1,2-thiazole-5-carboxylateHCID 13073192—
SolventChloroformHCID 6212—
ProductMethyl 4-iodo-3-phenylisothiazole-5-carboxylateHCID 5837416458.2%

Reaction Steps

To a solution of methyl 4-amino-3-phenylisothiazole-5-carboxylate (Preparation 103C, 700 mg, 2.99 mmol) in chloroform (80 mL) were added iodine (4019 mg, 15.84 mmol) and amyl nitrite (0.602 mL, 4.48 mmol). The resulting mixture was heated to reflux for 30 min. The reaction mixture was cooled to room temperature and washed with aqueous sodium thiosulfate and then water. The organic layer was dried over sodium sulfate. Removal of the solvent in vacuo and crystallization from ethanol yielded methyl 4-iodo-3-phenylisothiazole-5-carboxylate (600 mg, 1.738 mmol, 58.2% yield) as a pale yellow solid. The compound had an LC/MS M+1=346.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216972B2
Source datasetuspto-grants-2015_12
ORD IDord-6897a65a9f234ecab98806947d1450d7
Source noteuspto-grants-2015_12