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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389473Generated: November 1, 2026

Potassium Carbonate → Tert-butyl[2-(5-ethyloxycarbonyl-pentylsulfanyl)-benzoimidazol-1-yl]-acetate

https://huagongshe.com/reaction/2389473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 6-bromohexanoateHCID 117544—
ReactantHCID 178451223HCID 178451223—
SolventAcetoneHCID 180—
ProductTert-butyl[2-(5-ethyloxycarbonyl-pentylsulfanyl)-benzoimidazol-1-yl]-acetateHCID 9098754367.6%

Reaction Steps

A mixture of tert-butyl (2-mercapto-benzoimidazol-1-yl)-acetate (Intermediate 3-I, 52 mg, 0.2 mmol), 6-bromo-hexanoic acid ethyl ester (49 mg, 39 μl, 0.22 mmol) and K2CO3 (55 mg, 0.4 mmol) is refluxed in acetone (2 ml) for 5 h and stirred at rt overnight. Evaporation of the solvent in vacuo affords a residue that is purified by flash-chromatography on silica-gel (AcOEt/heptane, 25:75), yielding the title compound (55 mg) in 68% as a colourless oil: tR=7.24 min (LC-1), ESI-MS (pos.): m/z 407.23 [M+H]+, ESI-MS (neg.) 405.22 [M−H]+; 1H-NMR (CDCl3): δ (ppm) 1.25 (t, 3H CH3), 1.44 (s, 9H, tBu), 1.48 (m, 2H), 1.66 (quint., 2H), 1.79 (quint., 2H), 2.30 (t, 2H, CH2C═O), 3.38 (t, 2H, SCH2), 4.10 (q, 2H, OCH2), 4.73 (s, 2H, CH2CO2), 7.17-7.25 (m, 3Harom), 7.69 (m, 1Harom).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273740B2
Source datasetuspto-grants-2012_09
ORD IDord-105e05a2312545f28008739612e50b19
Source noteuspto-grants-2012_09