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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075164Generated: November 2, 2026

Acetic Anhydride → HCID 178503572, compound

https://huagongshe.com/reaction/1075164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantN-bromobutanimideHCID 67184—
Reactant4-Methylthio-5-bromo-6-methylpyrimid-2-oneHCID 20494288—
ReactantSodium BisulfiteHCID 23665763—
ReactantHCID 178503296HCID 178503296—
SolventAcetic AcidHCID 176—
ProductHCID 178503572HCID 17850357228%

Reaction Steps

4-Methylthiopyrimid-2-one (prepared as described in Wheller, L. H. and Johnson, B. T. J. Amer. Chem. Soc. 42 (1909) (30), (0.01 mol) was dissolved at ca. 80° C. in acetic acid (30 ml) containing 2% acetic anhydride. The temperature was lowered to ca. 55° C. and N-bromosuccinimide (0.013 mol) added and the reaction mixture stirred at this temperature for 40 min. Ice-cold water (150 ml) containing a little sodium bisulphite was then added and the precipitated collected and recrystallised from water; yield 28%, m.p. 260° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04395406
Source datasetuspto-grants-1983_07
ORD IDord-bc817db23ba34f979a11c43532a729f9
Source noteuspto-grants-1983_07