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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | Tert-butyl 4-(2-hydroxymethyl-3-methylbutyl)-2,2-dimethyloxazolidine-3-carboxylate | HCID 66888909 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl 4-(2-formyl-3-methylbutyl)-2,2-dimethyloxazolidine-3-carboxylate | HCID 86618882 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07868036B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-a81b7783e60f47d798116e7d9858815f |
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| Source note | uspto-grants-2011_01 |
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