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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73553Generated: October 29, 2026

Triethylamine → HCID 58386786, compound

https://huagongshe.com/reaction/73553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantHCID 58386792HCID 58386792—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 58386786HCID 5838678675%

Reaction Steps

To a solution of (3aR,7aS)-benzyl 2-oxohexahydrooxazolo[4,5-c]pyridine-5(6H)-carboxylate (1.0 equiv.) in dichloromethane (0.09 M) was added BOC2O (1.1 equiv.), triethylamine (1.1 equiv.), and a catalytic amount of DMAP. The reaction was stirred at room temperature for one hour at which point it was concentrated under vacuo and filtered through a plug of silica gel eluting with ethylacetate. The product was dried under vacuo to yield (3aR,7aS)-5-benzyl 3-tert-butyl 2-oxotetrahydrooxazolo[4,5-c]pyridine-3,5(2H,6H)-dicarboxylate as a white solid in 75% yield. LCMS (m/z): 277.2 (MH+), Rt=3.43 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829193B2
Source datasetuspto-grants-2014_09
ORD IDord-8ed3a0100a3348adb5b46efad76b795a
Source noteuspto-grants-2014_09