HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → cis-3,5-Diacetoxy-1-cyclopentene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | Cyclopentene, 3,5-dibromo-, cis- | HCID 10955247 | — |
| Catalyst | Hexadecyltrimethylammonium chloride | HCID 8154 | — |
| Product | cis-3,5-Diacetoxy-1-cyclopentene | HCID 10192610 | 77% |
Reaction Steps
One (1.0) g of cis-1,4-dibromocyclopent-2-ene, 3.5 g of potassium acetate, 0.7 g of cetyltrimethylammonium chloride, 5 ml of carbon tetrachloride, and 2 ml of water were used in the manner similar to the Example 1, at 42° C. for 6 hours. After addition of 30 ml of ether, the organic phase was dried over sodium sulfate, and the organic solvent was distilled off under a reduced pressure similarly to Example 1. Further subjecting the residual system to a reduced pressure distillation, 0.7 g of cis-1,4-diacetoxycyclopent-2-ene boiling at 60°-61° C./0.03 mmHg was obtained. The yield was 77%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04001308 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-e6073b52a36b456499751a41d07e08a0 |
| Source note | uspto-grants-1977_01 |