HuagongsheHuagongshe Chemistry Print Report · For research reference only
Vinyl ether → Thiophene, 2,2′-[thiobis(methylene)]bis-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Vinyl ether | HCID 8024 | — |
| Reactant | Thenyl mercaptan | HCID 80408 | — |
| Product | Thiophene, 2,2′-[thiobis(methylene)]bis- | HCID 54210762 | — |
Reaction Steps
f. Dithenyl sulfide was prepared by the same method as used for compound (1) b. (diethenyl ether) of Group X above, except that thenylmercaptan was used instead of thenyl alcohol. The product has a b.p. of 118°C./0.04 mm. Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03943260 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-b5b2d9c4b1314b0b96ded382154c946c |
| Source note | uspto-grants-1976_03 |