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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296183Generated: November 1, 2026

Sodium Thiosulfate → HCID 58911922, compound

https://huagongshe.com/reaction/1296183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 25808447HCID 25808447—
SolventDichloromethaneHCID 6344—
ProductHCID 58911922HCID 5891192226%

Reaction Conditions

Temperature0 °C

Reaction Steps

To 5-amino-2-(methylsulfanyl)-4-phenylthiazole (302 mg, 1.36 mmol) in dichloromethane (5.0 ml) was added portionwise 3-chloroperbenzoic acid (638 mg, 77% wt, 2.9 mmol) with cooling to 0° C. The mixture was diluted with dichloromethane (3.0 ml) and after 5 min allowed to warm to ambient temperature. After 3 hr a further quantity of 3-chloroperbenzoic acid (305 mg, 77% wt, 1.4 mmol) was added portionwise. After 20 hr the mixture was treated with sodium thiosulfate (2 ml, 1.0 M), poured into saturated aqueous sodium bicarbonate and extracted three times into dichloromethane (total 100 ml). The combined organic phases were washed with saturated aqueous sodium bicarbonate and brine, dried over sodium sulfate and concentrated in vacuo to give a dark brown foam. Flash chromatography on silica gel (ethyl acetate/hexanes) yielded pure 5-amino-2-(methylsulfonyl)-4-phenylthiazole (90 mg, 26%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244851B2
Source datasetuspto-grants-2007_07
ORD IDord-e1da09d10a8440e0bbf0c9f9078805ac
Source noteuspto-grants-2007_07