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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953963Generated: November 2, 2026

Benzyl Bromide → Methyl 3-Benzyloxy-5-(methylsulfonyl)-2-thiophenecarboxylate

https://huagongshe.com/reaction/1953963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 3-hydroxy-5-(methylsulfonyl)thiophene-2-carboxylateHCID 54724750—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-Benzyloxy-5-(methylsulfonyl)-2-thiophenecarboxylateHCID 1547709984%

Reaction Steps

A mixture of NaH (3.18 g, 79.5 mmol) in dimethylformamide (DMF) is treated dropwise with a solution of methyl 3-hydroxy-5-(methylsulfonyl)-2-thiophenecarboxylate (15.0 g, 63.6 mmol) in DMF at 0° C., stirred for 10 minutes, treated with benzylbromide (8.30 ml, 70 mmol) at ice bath temperatures, allowed to warm to room temperature overnight and diluted with water. The resultant reaction mixture is filtered. The filtercake is washed with water, dried, stirred in a mixture of ethyl acetate/hexane (20 ml/130 ml), and filtered. The filtercake is washed with hexanes and dried in a Kugelrohr at 40° C. to give the title product as a white solid, 17. 4 g (84% yield), mp 125-126° C. identified by 1HNMR, 13CNMR, IR and mass spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06121202
Source datasetuspto-grants-2000_09
ORD IDord-9681226c205345babd68f187519a3f51
Source noteuspto-grants-2000_09