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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1039920Generated: October 30, 2026

Toluene → 2-(2-Chloropyrimidin-4-yl)propan-2-ol

https://huagongshe.com/reaction/1039920

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactanttert-ButanolHCID 6386—
ReactantMethyl 2-chloropyrimidine-4-carboxylateHCID 43811076—
ReactantHCID 178418332HCID 178418332—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-(2-Chloropyrimidin-4-yl)propan-2-olHCID 7723106771%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of THF (0.25 mL) and toluene (1 mL) at −20° C. under a nitrogen atmosphere was added methyl magnesium chloride (3.0 M in THF, 1 mL, 2.90 mmol) followed by t-BuOH (0.050 mL in 0.750 mL THF, 0.579 mmol) and left to stir for 30 min at 0° C. The solution was cooled back down to −20° C. and methyl 2-chloropyrimidine-4-carboxylate (100 mg, 0.58 mmol) in THF (1 mL) was added. 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 2-(2-chloropyrimidin-4-yl)propan-2-ol (71 mg, 0.41 mmol, 71% yield. MS ESI: [M+H]+ m/z 173.1. 1H NMR (500 MHz, CDCl3) δ 8.60 (dd, J=1.8, 5.1, 1H), 7.44 (d, J=5.1 1H), 1.56 (d, J=1.8, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08551984B2
Source datasetuspto-grants-2013_10
ORD IDord-6536c52094b7478fbe50342373fa2bfe
Source noteuspto-grants-2013_10