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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065300Generated: October 30, 2026

Sodium Hydroxide → 2-(2-Furoylthio)acetamide

https://huagongshe.com/reaction/1065300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2-Furancarbonyl chlorideHCID 68242—
ReactantN-acetyl-2-(acetylthio)acetamideHCID 12837856—
SolventMethanolHCID 887—
Product2-(2-Furoylthio)acetamideHCID 20540299—

Reaction Conditions

Temperature0 °C

Reaction Steps

A slurry was prepared from 8.75 g. (0.05 mole) of N-acetyl-2-(acetylthio)acetamide and 100 ml. of methanol at -5° C., and nitrogen was bubbled through the slurry. There was then added 2.0 g. (0.05 mole) of sodium hydroxide in 20 ml. of methanol. The reaction mixture was aged for 1 hour and then concentrated under high vacuum while the temperature was kept below 30° C. Next, 100 ml. of dimethylformamide was added and the reaction mixture was cooled to 0° C. There was then added 7.2 g. (0.055 mole) of 2-furoyl chloride, and the reaction mixture was aged for 3 hours at 0° C., after which it was concentrated under high vacuum. The residue was charged to a silica gel column and eluted with 50% ethylacetate/hexane. The product was recrystallized from toluene and air dried to yield 2.9 g., m.p. 126°-128° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04329363
Source datasetuspto-grants-1982_05
ORD IDord-ed99dd1653194b009c1574a4b55eb24b
Source noteuspto-grants-1982_05