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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1039926Generated: October 31, 2026

(2-Chloropyrimidin-4-yl)(cyclopropyl)methanone → 1-(2-Chloropyrimidin-4-yl)-1-cyclopropylethanol

https://huagongshe.com/reaction/1039926

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Chloropyrimidin-4-yl)(cyclopropyl)methanoneHCID 77231065—
ReactantHCID 178418332HCID 178418332—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1-(2-Chloropyrimidin-4-yl)-1-cyclopropylethanolHCID 7723106460.4%

Reaction Steps

To a solution of (2-chloropyrimidin-4-yl)(cyclopropyl)methanone (175 mg, 0.958 mmol) in THF (3 mL) at −78° C. under a nitrogen atmosphere was added methyl magnesium chloride (3.0 M in diethyl ether, 0.380 mL, 1.15 mmol) dropwise. The solution was warmed to room temperature and stirred for an additional 30 min. The solution was diluted with EtOAc, washed with brine, dried with MgSO4, filtered, and concentrated to dryness to afford 1-(2-chloropyrimidin-4-yl)-1-cyclopropylethanol (115 mg, 0.579 mmol, 60% yield). MS ESI: [M+H]+ m/z 199.1. 1H NMR (500 MHz, CDCl3) δ 8.60 (d, J=5.2, 1H), 7.43 (d, J=5.2, 1H), 3.43 (s, 1H), 1.52 (s, 3H), 1.26 (m, 1H), 0.60 (m, 1H), 0.50 (m, 1H), 0.40 (m, 1H), 0.30 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08551984B2
Source datasetuspto-grants-2013_10
ORD IDord-0c474cc456f94917a942c12f16407ef9
Source noteuspto-grants-2013_10