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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422177Generated: October 25, 2026

Dimethylformamide → Methyl (3-benzyloxy-5-trifluoromethylthien-2-yl)-carboxylate

https://huagongshe.com/reaction/1422177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 3-hydroxy-5-(trifluoromethyl)thiophene-2-carboxylateHCID 2759855—
SolventWaterHCID 962—
ProductMethyl (3-benzyloxy-5-trifluoromethylthien-2-yl)-carboxylateHCID 1127850864%

Reaction Steps

A mixture of 1B (5.0 g) and dimethylformamide (50 ml) is treated with sodium hydride (1.06 g). Benzylbromide (3.15 ml) was slowly added to the resulting reaction mixture and stirred at room temperature for 20 hours. The reaction mixture was poured into water. The mixture was extracted with diethyl ether twice. The combined organic phases were washed with water, dried and concentrated in vacuo. The crude product was chromatographed (hexane/dichloromethane, 1/1) to give the product as a white solid (4.5 g, 64%) with a melting point of 52-53.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06080861
Source datasetuspto-grants-2000_06
ORD IDord-5d07badda3e04b65bf8ddf1aeedc618b
Source noteuspto-grants-2000_06