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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367052Generated: October 30, 2026

Water → {[4-(Trifluoromethyl)pyridin-2-yl]methoxy}acetic Acid

https://huagongshe.com/reaction/2367052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl bromoacetateHCID 79177—
Reactant2-(Hydroxymethyl)-4-(trifluoromethyl)pyridineHCID 14761459—
SolventDimethylformamideHCID 6228—
Product{[4-(Trifluoromethyl)pyridin-2-yl]methoxy}acetic AcidHCID 57803266—

Reaction Steps

To a solution of [4-(trifluoromethyl)pyridin-2-yl]methanol (340 mg, 1.9 mmol) in DMF (10 mL) was added sodium hydride (150 mg, 3.8 mmol). After being stirred at room temperature for 5 min. 1,1-dimethylethyl bromoacetate (0.28 mL, 1.9 mmol) was added. Stirring was continued at room temperature for 1 h. Water (20 mL) was added and the resulting solution was extracted with EtOAc. The water layer was neutralized to pH=5 with HCl and extracted with EtOAc twice. The combined organic layers were dried (MgSO4) and concentrated under vacuum to give the title compound which was used for the next reaction without purification. MS (M+H) 292.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697870B2
Source datasetuspto-grants-2014_04
ORD IDord-3f78b1e6b3da430093d9843f79d1905a
Source noteuspto-grants-2014_04