HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 2-ethylsulfanylpyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 178418616 | HCID 178418616 | — |
| Product | 2-ethylsulfanylpyridine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04085109 |
| Source dataset | uspto-grants-1978_04 |
| ORD ID | ord-788b5fe6a9bb4ef3a9f3035b6540daf4 |
| Source note | uspto-grants-1978_04 |