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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727167Generated: November 1, 2026

Isopropenyl chloroformate → HCID 10326313, compound

https://huagongshe.com/reaction/1727167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropenyl chloroformateHCID 93846—
ReactantHCID 86614040HCID 86614040—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 10326313HCID 1032631396.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To (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, 0.096 mmol) and 4-dimethylaminopyridine (35 mg, 0.29 mmol) in dichloromethane (5 ml) at 0° C. under nitrogen was added isopropenyl chloroformate (17.4 mg, 0.144 mmol) and the resulting mixture stirred at 0° C. for 30 minutes and at room temperature for 2 hours. The reaction mixture was diluted with dichloromethane (25 ml) and washed with citric acid solution (3×15 ml), dried (MgSO4) and concentrated in vacuo. The crude product was purified by chromatography on silica (5 g) eluting with hexane:ethyl acetate (1:1). The pure fractions were combined and concentrated in vacuo to give the title product (56 mg, 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07494992B2
Source datasetuspto-grants-2009_02
ORD IDord-b0cd34d36572401c8d00f8d5aa66a69d
Source noteuspto-grants-2009_02