HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78752Generated: October 26, 2026
Hydrochloric Acid → Hexahydrofuro(2,3-b)furan-3-ol
https://huagongshe.com/reaction/78752
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | HCID 67609631 | HCID 67609631 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Hexahydrofuro(2,3-b)furan-3-ol | HCID 9898832 | 46.6% |
Reaction Steps
2 M Lithium borohydride solutions (24.7 ml) was added to the flask under nitrogen atmosphere. Ethyl-2-(2-methoxytetrahydrofuran-3-yl)-2-oxoacetate (5 g) was dissolved in THF (25 ml) and slowly added at 65-70° C. Reaction mass was then maintained at 65-70° C. for 10 hrs. Reaction mass was cooled to −10° C. and slowly added concentrated hydrochloric acid (16 ml) and stirred for 2 hrs at −5 to 0° C. Triethyl amine (14.6 ml) was added to the reaction mass. Reaction mass was concentrated under vacuum. Ethyl acetate (20 ml) was added and again concentrated to residue. Ethyl acetate (50 ml) was added to it and filtered the un-dissolved salts. Filtrate was concentrated to get residue of Hexahydrofuro[2,3-b]furan-3-ol (yield 1.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841467B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-7de6b855cac942bb8cde562ed1da7b6a |
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| Source note | uspto-grants-2014_09 |
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