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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23754Generated: October 26, 2026

Ethanol → 2-({2H,3H-thieno[3,4-b][1,4]dioxin-2-yl}methoxy)acetic acid

https://huagongshe.com/reaction/23754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium HydroxideHCID 14797—
Reactant(2,3-Dihydro-thieno[3,4-b][1,4]dioxin-2-ylmethoxy)-acetic acid ethyl esterHCID 20758020—
SolventWaterHCID 962—
Product2-({2H,3H-thieno[3,4-b][1,4]dioxin-2-yl}methoxy)acetic acidHCID 21958361—

Reaction Conditions

Temperature35 °C

Reaction Steps

(2,3-Dihydro-thieno[3,4-b][1,4]dioxin-2-ylmethoxy)-acetic acid ethyl ester (10.2 g, 40 mmol) was dissolved into ethanol (100 mL) and water (50 mL), blanketed by nitrogen. Potassium hydroxide (2.9 g) was added and the mixture was heated at 35° C. for 30 min. The solvents were then removed by distillation, ethyl acetate (50 mL), ice-water (50 mL) and concentrated hydrochloric acid (5 mL) were added and the mixture was vigorously stirred. Subsequently, the organic phase was separated, washed with a saturated aqueous solution of sodium chloride, dried with anhydrous magnesium sulphate and concentrated. Finally the raw product was recrystallized from ethyl acetate/hexanes (1/1) resulting in pure (2,3-dihydro-thieno[3,4-b][1,4]dioxin-2-ylmethoxy)-acetic acid as demonstrated by NMR and mass spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852830B2
Source datasetuspto-grants-2005_02
ORD IDord-2cc39ed64f4449049f9985573de4f08e
Source noteuspto-grants-2005_02