HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Epoxybutane → HCID 12788552, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Epoxybutane | HCID 7834 | — |
| Reactant | HCID 12651433 | HCID 12651433 | — |
| Reactant | HCID 86735152 | HCID 86735152 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 12788552 | HCID 12788552 | 58% |
Reaction Steps
A mixture of 2.36 g. (9.54 mmol) of 2,3,6-trichloro-4-methoxybenzyl triphenylphosphonium chloride and 2.0 g. (8.93 mmol) of ethyl (E,Z,E)-4-fluoro-3,7-dimethyl-8-oxo-2,4,6-octatrienoate in 200 ml. of toluene and 150 ml. of 1,2-butylene oxide was heated at 85°-90° C. under argon for 18 hours. The mixture was worked up in the usual manner and the resulting crude product was filtered through 150 g. of silica gel. Elution with methylene chloride gave 2.48 g. of a yellow crystalline substance. Recrystallization of this material from methylene chloride-isopropyl ether yielded 2.21 g. (58% yield) of ethyl (E,Z,E,E)-9-(2,3,6-trichloro-4-methoxyphenyl)-4-fluoro-3,7-dimethyl-2,4,6,8-nonatetraenoate as yellow crystals, mp. 140°-142.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04171318 |
| Source dataset | uspto-grants-1979_10 |
| ORD ID | ord-32963b385a80427eae9436a91a4208b8 |
| Source note | uspto-grants-1979_10 |