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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059958Generated: October 25, 2026

Diethyl Ether → ethyl [(1-benzyl-1H-benzimidazol-2-yl)sulfanyl]acetate

https://huagongshe.com/reaction/2059958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantBenzyl BromideHCID 7498—
Reactantethyl 2-(1H-1,3-benzodiazol-2-ylsulfanyl)acetateHCID 21564—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Productethyl [(1-benzyl-1H-benzimidazol-2-yl)sulfanyl]acetateHCID 97543131%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of ethyl 2-(1H-benzo[d]imidazol-2-ylthio)acetate 4a (11.2 g, 47.6 mmol, 1.0 eq.) in 10:1 diethyl ether:dimethylformamide (450 mL) at 0° C., was added 60% sodium hydride in mineral oil (2.09 g, 52.3 mmol, 1.1 eq.), and the reaction was stirred at 0° C. for 20 minutes. Benzyl bromide (9.78 g, 57.1 mmol, 1.2 eq.) was added at 0° C., and the reaction was stirred with warming to room temperature for 16 hours. The reaction mixture was quenched with methanol (100 mL) and concentrated in vacuo. The residue was taken into hot chloroform (400 mL) and filtered. The filtrate was washed with water (200 mL), 1M HCl (200 mL) and brine (200 mL). The organic layer was dried over magnesium sulfate and concentrated in vacuo. Purification by flash chromatography (10% EtOAc:90% petroleum ether) gave 4b as a pale-yellow solid (4.82 g, 30%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278327B2
Source datasetuspto-grants-2012_10
ORD IDord-78ec53df199c44c4b210f4fb9b37d8e2
Source noteuspto-grants-2012_10