HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Butadiene → 1,3-Butadiene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Butadiene | HCID 7845 | — |
| Reactant | Dicofol | HCID 8268 | — |
| Product | 1,3-Butadiene | HCID 7845 | — |
| Product | Vinyloxirane | HCID 13586 | — |
Reaction Steps
CPCA is derived from 1,3-butadiene by a sequence of four reactions. Monoepoxidation of 1,3-butadiene produces 3,4-epoxy-1-butene (EPB) as described in U.S. Pat. Nos. 4,897,498 and 4,950,773. This epoxide is isomerized to 2,5-DHF (U.S. Pat. Nos. 5,082,956 and 5,315,019) which is isomerized to 2,3-DHF (U.S. Pat. Nos. 5,254,701 and 5,536,851). Finally, 2,3-DHF is isomerized to CPCA (C. L. Wilson, J. Amer. Chem. Soc., 69, 3002 (1947) and U.S. Pat. No. 5,502,257).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06353140B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-5cb8ae1cdedb45b5a7df1440ce203d52 |
| Source note | uspto-grants-2002_03 |