Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383886Generated: November 1, 2026

Acetone → HCID 59636235, compound

https://huagongshe.com/reaction/2383886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantEthyl AcetateHCID 8857—
Reactant3-BromopyridineHCID 12286—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 59636235HCID 5963623541.8%

Reaction Conditions

Temperature-10 °C

Reaction Steps

Butyl Lithium (10.28 mL, 16.455 mmol) was added to a solution of DIPA (2.66 mL, 18.98 mmol) in THF (25 mL) at -78° C. The reaction mixture was stirred at -10° C. for 10 minutes, followed by the addition of 3-bromo-pyridine (500 mg, 2.212 mmol) in THF (10 mL) at -100° C. The reaction mixture was stirred for a further 15 minutes at -90° C. and was followed by the addition of acetone (1.675 mL, 22.78 mmol) in THF (10 mL) at -78° C. with stirring over a period of 1 hour. The reaction was monitored by TLC (5% ethylacetate in hexane). The reaction mixture was quenched with aqueous NaHCO3 solution and extracted with ethylacetate. The organic layer was dried over Na2SO4 and concentrated. Purification by column chromatography on silica gel (15% ethylacetate in hexane) afforded 200 mg of 2-(3-bromo-pyridin-4-yl)-propan-2-ol (11% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263635B2
Source datasetuspto-grants-2012_09
ORD IDord-14986f65cc1e4ebab0a3d024c4e532a8
Source noteuspto-grants-2012_09