HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223986Generated: October 26, 2026
Ethanol → 2-({2H,3H-thieno[3,4-b][1,4]dioxin-2-yl}methoxy)acetic acid
https://huagongshe.com/reaction/2223986
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | (2,3-Dihydro-thieno[3,4-b][1,4]dioxin-2-ylmethoxy)-acetic acid ethyl ester | HCID 20758020 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-({2H,3H-thieno[3,4-b][1,4]dioxin-2-yl}methoxy)acetic acid | HCID 21958361 | — |
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 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07378039B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-f127bad01afb4a75816376f73b436196 |
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| Source note | uspto-grants-2008_05 |
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