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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874875Generated: October 28, 2026

Methanesulfonic Acid → (4-chloro-2-propyl-1H-imidazol-5-yl)methanol

https://huagongshe.com/reaction/1874875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantSodium HydroxideHCID 14798—
Reactant4-chloro-5-{[(phenylmethyl)oxy]methyl}-2-propyl-1H-imidazoleHCID 59451389—
SolventChloroformHCID 6212—
Product(4-chloro-2-propyl-1H-imidazol-5-yl)methanolHCID 1037492482%

Reaction Steps

A solution of 4-chloro-5-{[(phenylmethyl)oxy]methyl}-2-propyl-1H-imidazole (1.72 g, 6.5 mmol) and methanesulfonic acid (16 mL, 247 mmol) in chloroform (36 mL) was stirred at RT for 1 h. The reaction mixture was poured into ice (˜70 g) and the solution was neutralized by addition of 5N NaOH until the pH was 10. The solution was extracted with methyl tert-butyl ether (2×60 mL) and then with n-butanol (3×40 mL). The combined n-butanol extracts were concentrated, washed with brine, and dried in vacuo to provide the title compound (0.927 g, 82%) as a light yellow solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 12.09 (br. s., 1H), 5.10 (br. s., 1H), 4.31 (s, 2H), 2.45-2.51 (m, 2H), 1.60 (sex, 2H), 0.87 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-4fe9f3c5e8a54e7d8f1da7be70a7fa81
Source noteuspto-grants-2012_11