HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → Oxacyclotridecan-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Cyclododecanone | HCID 13246 | — |
| Product | Oxacyclotridecan-2-one | HCID 70354 | 75% |
Reaction Steps
Cyclododecanone was treated with trifluoroacetic acid to form the lactone (Huisgen, R. et al., ibid), dodecanolid (yield 75%; bp 111°-115° C. at 8 mm). The lactone was hydrolyzed to form 12-hydroxydodecanoic acid (Smissman, E. et al., ibid) (yield 92%; mp 82°-4° C.). The hydroxy acid was converted to 12-bromododecanoic acid (VI) with 48% HBr in the presence of H2SO4 (Jocelyn, P. et al., ibid) (yield 88%; mp 52°-55° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04845271 |
| Source dataset | uspto-grants-1989_07 |
| ORD ID | ord-c1cc0b085e674433814df35b1351cfb3 |
| Source note | uspto-grants-1989_07 |