HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl chloroformate → HCID 53895456, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl chloroformate | HCID 61140 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | Acetic Acid 3-(4-tert-butyl-phenyl)-2-methyl-propenyl Ester | HCID 53757095 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53895456 | HCID 53895456 | — |
Reaction Steps
A solution of 40.0 g acetic acid 3-(4-tert-butyl-phenyl)-2- methyl-propenyl ester in 250 ml of THF was cooled to −70° C. A solution of 25.0 g potassium-tert-butoxide in 100 ml of THF was added at −70° C. during 35 min. and the resulting reaction mixture was stirred for 60 min. at the same temperature. 23.3 g butyl-chloroformate was dropped in during 40 min. and the reaction mixture was stirred for another 90 min. at −70° C. Then the reaction mixture was diluted with ether, washed with saturated NaHCO3 and brine. The organic phase was dried, filtered and evaporated to dryness. The residue was thin-layer distilled and purified by chromatography to yield a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06232487B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-17a9130549314661b83c2e7ad49881ce |
| Source note | uspto-grants-2001_05 |