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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252402Generated: October 30, 2026

Triethylamine → Tert-butyl 4-(2-formyl-3-methylbutyl)-2,2-dimethyloxazolidine-3-carboxylate

https://huagongshe.com/reaction/252402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPotassium bisulfateHCID 516920—
ReactantTert-butyl 4-(2-hydroxymethyl-3-methylbutyl)-2,2-dimethyloxazolidine-3-carboxylateHCID 66888909—
SolventDimethyl SulfoxideHCID 679—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-(2-formyl-3-methylbutyl)-2,2-dimethyloxazolidine-3-carboxylateHCID 86618882—

Reaction Conditions

Temperature0 °C

Reaction Steps

6.97 ml of triethylamine are added dropwise at 0° C. to the solution of 3.0 g of tert-butyl 4-(2-hydroxymethyl-3-methylbutyl)-2,2-dimethyloxazolidine-3-carboxylate in 11 ml of dimethyl sulphoxide and 55 ml of dichloromethane. 5.23 g of sulphur trioxide-pyridine complex are added in 3 portions at intervals of 10 minutes and the reaction mixture is stirred at 0° C. for a further 3 hours. The reaction mixture is poured onto ice-water, adjusted to pH=2.5 with saturated aqueous potassium bisulphate solution and extracted with diethyl ether (3×)—the combined organic phases are washed successively with water and 5% aqueous sodium hydrogencarbonate solution, dried over sodium sulphate and concentrated by evaporation. The title compound is obtained from the residue as a yellow oil. Rf=0.46 (1:2 EtOAc-heptane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868036B2
Source datasetuspto-grants-2011_01
ORD IDord-a81b7783e60f47d798116e7d9858815f
Source noteuspto-grants-2011_01