Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083258Generated: November 1, 2026

Acetic Anhydride → 2-ethylsulfanylpyridine

https://huagongshe.com/reaction/2083258

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 178418616HCID 178418616—
Product2-ethylsulfanylpyridineHCID 412543—

Reaction Steps

d. 2-Ethylthio-pyridine was prepared by the same method as used for compound (1) c., except that ethyl halide was used instead of methyl halide. The product had a b.p. of 77°-77.5° C./8 mm. Hg. (1) e. (Pyridyl-2)-thiol acetate was prepared by reacting acetic anhydride with 2-mercaptopyridine in alkaline medium according to the method described in Houben-Weyl, 4th ed., vol. 9, 753 (1955) and in J.A.C.S. 59, 1089 (1937). The product has a b.p. of 117°-118° C./9 mm. Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04085109
Source datasetuspto-grants-1978_04
ORD IDord-788b5fe6a9bb4ef3a9f3035b6540daf4
Source noteuspto-grants-1978_04