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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175126Generated: October 30, 2026

Ammonium Chloride → HCID 67255249, compound

https://huagongshe.com/reaction/2175126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde, (S)-(-)-HCID 179824—
ReactantHCID 178418797HCID 178418797—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67255249HCID 67255249—

Reaction Conditions

Temperature-78 °C

Reaction Steps

5 g (21.81 mmol) of (S)-4-formyl-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester are dissolved in 33 ml of THF, placed under argon and cooled to −78° C. 43.62 ml (21.81 mmol) of a 0.5 M 3-butenylmagnesium bromide solution in THF are added dropwise. The mixture is stirred further at room temperature overnight. After TLC check, about 90 ml of a saturated NH4Cl solution are added to the mixture with cooling, the mixture is stirred further overnight and diluted with about 50 ml of water. The phases are separated, and the aqueous phase is extracted a further twice with EA. The combined organic phases are dried over sodium sulfate, filtered and evaporated. The oily residue is subjected to flash chromatography on silica gel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062015B2
Source datasetuspto-grants-2015_06
ORD IDord-767afb79c7dc4c229f828da06a10a482
Source noteuspto-grants-2015_06