HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl chloroformate → HCID 11196464, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl chloroformate | HCID 18052 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Eglumegad | HCID 213056 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 11196464 | HCID 11196464 | 67.3% |
Reaction Steps
(1S,2S,5R,6S)-2-Amino-bicyclo[3.1.0]hexane-2,6-dicarboxylic acid (15.0 g, 73.9 mmol) was slowly dissolved in 250 mL of saturated sodium bicarbonate. After complete solution, dioxane (100 mL) and allyl chloroformate (15.7 mL, 147.8 mmol) were added at room temperature and the mixture was stirred overnight. The reaction mixture was diluted with water (100 mL) and washed with three portions of ethyl acetate. The organic layer was extracted once with saturated sodium bicarbonate. The combined aqueous layers were acidified to pH 1 with 4N hydrochloric acid and extracted with two portions of ethyl acetate. The organic layer was dried over magnesium sulfate, filtered and concentrated to provide the title compound as an oil (13.4 g, 67% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07038077B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-ea2200241666465fb9e98748c21262a2 |
| Source note | uspto-grants-2006_05 |