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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207052Generated: October 31, 2026

Pivaloyl chloride → (S)-2-(5-bromo-2,7-dimethylquinolin-6-yl)-2-hydroxyethyl pivalate

https://huagongshe.com/reaction/2207052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPivaloyl chlorideHCID 62493—
Reactant(S)-1-(5-bromo-2,7-dimethylquinolin-6-yl)ethane-1,2-diolHCID 66633145—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product(S)-2-(5-bromo-2,7-dimethylquinolin-6-yl)-2-hydroxyethyl pivalateHCID 66631779—

Reaction Steps

To a stirred solution of (S)-1-(5-bromo-2,7-dimethylquinolin-6-yl)ethane-1,2-diol (290 mg, 0.98 mmol) in dichloromethane (12 mL) and pyridine (2 mL) was added trimethyl acetylchloride (0.24 mL, 1.97 mmol) at 0° C. The mixture was stirred at room temperature for 2 hours, and quenched with slow addition of NaHCO3 solution. The mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried and concentrated in vacuo. The obtained residue was purified by flash chromatography to provide (S)-2-(5-bromo-2,7-dimethylquinolin-6-yl)-2-hydroxyethyl pivalate. LCMS-ESI+ (m/z): [M+H]+ calc'd for C18H23BrNO3: 380.1; Found: 380.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376392B2
Source datasetuspto-grants-2016_06
ORD IDord-74ba0a8e0a9b4f858e2141a527e5d981
Source noteuspto-grants-2016_06