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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044419Generated: November 3, 2026

Sodium Methoxide → (5-Chloropyridin-2-yl)methanol

https://huagongshe.com/reaction/1044419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 58580279HCID 58580279—
SolventMethanolHCID 887—
Product(5-Chloropyridin-2-yl)methanolHCID 2053789359%

Reaction Steps

Sodium methoxide (1M in MeOH) (0.162 mL, 0.162 mmol) was added to a solution of (5-chloropyridin-2-yl)methyl benzoate Part C (200 mg, 0.808 mmol) in MeOH (47.5 mL) and stirred at RT for 2.0 h. The solvent was removed in vacuo and the crude product was subjected to flash chromatography (silica gel/DCM-MeOH 100:0 to 90:10 gradient) to afford (5-chloropyridin-2-yl)methanol 16D (68 mg, 59% yield) as an off-white solid. LC-MS, [M+H]+=144. 1H NMR (400 MHz, DMSO) δ 8.51 (1H, d, J=2.2 Hz), 7.91 (1H, dd, J=8.4, 2.6 Hz), 7.49 (1H, d, J=8.4 Hz), 5.53 (1H, t, J=5.9 Hz), 4.54 (2H, d, J=6.2 Hz). HPLC-Method 8; 0.76 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563583B2
Source datasetuspto-grants-2013_10
ORD IDord-f67a7bfcce0c440d8155c81c562a1657
Source noteuspto-grants-2013_10