HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354106Generated: November 1, 2026
Hydrochloric Acid → 2-Hydroxymethyl-chroman-4-one
https://huagongshe.com/reaction/354106
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-oxo-3,4-dihydro-2H-1-benzopyran-2-carboxylic acid | HCID 9855708 | — |
| Reactant | (Dimethyl sulfide)trihydroboron | HCID 12423031 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Hydroxymethyl-chroman-4-one | HCID 14089213 | 93.5% |
Reaction Steps
The 3 g of 4-oxo-chromane-2-carboxylic acid in THF (65 mL) was stirred was cooled to 0° C. and borane-methyl sulfide complex (2.5 mL of M solution, 25 mmoles) was added dropwise for about 15 minutes. The solution was warmed to room temperature and then heated at reflux for 4 hours. The solution was cooled to room temperature and 10% aqueous hydrochloric acid (20 mL) was added over 15 minutes and the solution was stirred at room temperature for 2 hours. The mixture was concentrated to approximately 25 mL. The solution was poured into ethyl acetate (50 mL) and washed with water (2×30 mL), saturated sodium bicarbonate (2×30 mL) and saturated ammonium chloride (2×30 mL). The organic layer was separated dried over anhydrous MgSO4, and then concentrated in vacuo to yield about 2.6 g of 2-(hydroxymethyl)-chroman-4-one (86.7% yield)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06756403B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-e1b2f3182738448d9ff1217443bfb034 |
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| Source note | uspto-grants-2004_06 |
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