HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727168Generated: November 4, 2026
Allyl chloroformate → HCID 10031568, compound
https://huagongshe.com/reaction/1727168
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl chloroformate | HCID 18052 | — |
| Reactant | HCID 86614040 | HCID 86614040 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10031568 | HCID 10031568 | 76% |
Reaction Steps
Allyl chloroformate (17.4 mg) was added to a stirred, cooled (0° C.) solution of (1S,4aS,5S,8aR)-2,8a-dihydroxy-3,8-dimethyl-5-(1-methylethyl)-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl (2S,3aR,9bR)-6-chloro-9b-hydroxy-5-methyl-1,2,3,3a,5,9b-hexahydropyrrolo[2,3-c][2,1]benzoxazine-2-carboxylate (Preparation 144, 50 mg) and 4-dimethylaminopyridine (35 mg) in dichloromethane (5 ml) under an atmosphere of nitrogen. After 30 minutes, the reaction was allowed to warm to room temperature over 15 hours. The reaction mixture was diluted with dichloromethane (25 ml), washed with aqueous citric acid (10% w/w, 3×15 ml) and dried (MgSO4). After evaporation of solvent in vacuo, the residue was purified by flash column chromatography on silica (5 g) eluting with 1:1 ethyl acetate:hexane to give the product (44 mg, 76%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07494992B2 |
|---|
| Source dataset | uspto-grants-2009_02 |
|---|
| ORD ID | ord-f2a5ed5f1eaa4da0abd7e9a8ad2d4770 |
|---|
| Source note | uspto-grants-2009_02 |
|---|