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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727213Generated: November 3, 2026

Triethylamine → HCID 69056915, compound

https://huagongshe.com/reaction/1727213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 86614034HCID 86614034—
SolventMethanolHCID 887—
ProductHCID 69056915HCID 69056915—

Reaction Steps

A solution of (1S,2R,4aS,5R,8R,8aR)-2-(acetyloxy)-8a-hydroxy-3,8-dimethyl-5-(1-methylethenyl)-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 1, 100 g) and triethylamine (10 ml) in methanol (1000 ml) was stirred at room temperature for 3 hours. The reaction mixture was evaporated and the residue was crystallised from ethyl acetate/hexane to give a pure sample of the terpene, (1S,2R,4aR,5R,8S,8aS)-1,8a-dihydroxy-5-isopropenyl-3,8-dimethyl-1,2,4a,5,6,7,8,8a-octahydro-2-naphthalenyl acetate (Preparation 126). The remaining solution was concentrated and purified by flash column chromatography on silica-gel eluting with ethyl acetate:dichloromethane:hexane (2:1:7) to give further terpene moiety (1S,2R,4aR,5R,8S,8aS)-1,8a-dihydroxy-5-isopropenyl-3,8-dimethyl-1,2,4a,5,6,7,8,8a-octahydro-2-naphthalenyl acetate as a white solid (Preparation 126, 43 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07494992B2
Source datasetuspto-grants-2009_02
ORD IDord-b525d2242fe4472b8140693a4272d6ff
Source noteuspto-grants-2009_02