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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727168Generated: November 4, 2026

Allyl chloroformate → HCID 10031568, compound

https://huagongshe.com/reaction/1727168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl chloroformateHCID 18052—
ReactantHCID 86614040HCID 86614040—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 10031568HCID 1003156876%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07494992B2
Source datasetuspto-grants-2009_02
ORD IDord-f2a5ed5f1eaa4da0abd7e9a8ad2d4770
Source noteuspto-grants-2009_02