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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389469Generated: November 1, 2026

Potassium Carbonate → Tert-butyl[2-(2-methoxy-benzylsulfanyl)-benzoimidazol-1-yl]-acetate

https://huagongshe.com/reaction/2389469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Chloromethyl)anisoleHCID 81495—
ReactantHCID 178451223HCID 178451223—
SolventAcetoneHCID 180—
ProductTert-butyl[2-(2-methoxy-benzylsulfanyl)-benzoimidazol-1-yl]-acetateHCID 9090708263.8%

Reaction Steps

A suspension of K2CO3 (31.4 mg, 0.23 mmol) in acetone (3 ml) containing tert-butyl (2-mercapto-benzoimidazol-1-yl)-acetate (Intermediate 3-I, 30 mg, 0.11 mmol) and 2-methoxybenzyl chloride (17.8 mg, 15.8 μl, 0.11 mmol) is stirred at rt overnight. Filtration over Celite and evaporation of the solvent in vacuo affords the pure title compound (27 mg) in 62% yield as a yellow oil: tR=7.47 min (LC-1), MS (pos.): m/z 385.20 [M+H]+; 1H NMR (DMSO-d6): δ (ppm) 1.37 (s, 9H, tBu), 3.90 (s, 3H, OCH3), 4.53 (s, 2H, SCH2), 4.92 (s, 2H, CH2CO2), 6.87 (t, 1Harom), 7.03 (d, 1Harom), 7.21 (m, 2Harom), 7.28 (t, 1Harom), 7.40 (d, 1Harom), 7.50 (m, 1Harom), 7.64 (m, 1Harom).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273740B2
Source datasetuspto-grants-2012_09
ORD IDord-086a1f7b873e419c8bfdb9b685b6f8f0
Source noteuspto-grants-2012_09