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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386918Generated: November 1, 2026

Pivaloyl chloride → HCID 70238042, compound

https://huagongshe.com/reaction/1386918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPivaloyl chlorideHCID 62493—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 69624824HCID 69624824—
SolventEthyl AcetateHCID 8857—
SolventOxolane--water (1/1)HCID 21881883—
ProductHCID 70238042HCID 70238042137.9%

Reaction Steps

To the solution of (2S,3R)-3-(4-hydroxyphenyl)pyrolidine-2-carboxylic acid methyl ester hydrochloride (200 mg, 0.76 mmol), prepared in Example 20, in THF/H2O (2 mL/1 mL) was added saturated NaHCO3 (5 mL). To the above mixture was added trimethylacetyl chloride (420 mg, 3.5 mmol) over 20 min. The resulting solution was then stirred at room temperature for 4 hours and was diluted with ethyl acetate to 30 mL. The organic layer was then washed with brine (2×5 mL) and was concentrated to give (2S,3R)-1-(1-oxo-2,2,2-trimethylethyl)-3-(4-hydroxyphenyl)pyrolidine-2-carboxylic acid methyl ester as a white solid (320 mg). This solid was dissolved in 3 mL of EtOH and was stirred with 1N sodium hydroxide (3 mL, 3 mmol) at room temperature for 8 hours. After acidification with 6N HCl, the solvent was removed and the residue was extracted with dichloromethane. After concentration, the residue was washed ether to give (2S,3R)-1-(2,2-dimethyl-1-oxopropyl)-3-(4-hydroxyphenyl)pyrolidine-2-carboxylic acid as a white solid (117 mg). HRMS (M+H): Obs. 292.1556, Cald. 292.1549.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265572B1
Source datasetuspto-grants-2001_07
ORD IDord-3e593ab042b448e0a8503a793281fdd6
Source noteuspto-grants-2001_07