HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093468Generated: November 1, 2026
Hydrochloric Acid → 3-(2,3-Dihydro-1-benzofuran-5-yl)propan-1-ol
https://huagongshe.com/reaction/1093468
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | 3-(2,3-Dihydro-1-benzofuran-5-yl)propanoic acid | HCID 2815405 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(2,3-Dihydro-1-benzofuran-5-yl)propan-1-ol | HCID 53425002 | 103% |
Reaction Steps
3-(2,3-Dihydrobenzofuran-5-yl)propionic acid (2.00 g) was dissolved in tetrahydrofuran (20 ml), and a tetrahydrofuran-borane.tetrahydrofuran solution (1 mol/l, 11.5 ml) was added dropwise to the mixture under ice-cooling. The mixture was stirred under ice-cooling for 1 hr, and further at room temperature for 16 hr. Water was added to the reaction mixture, and 1M aqueous hydrochloric acid solution was added. The mixture was extracted with ethyl acetate, washed with water, saturated aqueous sodium hydrogen carbonate solution and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to give the object product (1.91 g) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129361B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-92bd6c83ced041d09f489f479e3424ed |
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| Source note | uspto-grants-2012_03 |
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