HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 367276Generated: October 28, 2026
Acetone → (2R)-3,4-Dihydro-2H-1-benzopyran-2-methanol
https://huagongshe.com/reaction/367276
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Water | HCID 962 | — |
| Product | (2R)-3,4-Dihydro-2H-1-benzopyran-2-methanol | HCID 7170029 | — |
Reaction Steps
A mixture of toluene (1000 ml) and ethanol (absolute, 520 ml) was stirred. Sodium borohydride (2.13 mol) was added at room temperature, under an inert atmosphere. The mixture was heated to 50° C. Intermediate (2) (2.14 mol) was added dropwise at 50° C. in a 90-minutes period (exothermic temperature rise of 15° C.; cooling required). The reaction mixture was stirred for 90 minutes at 50° C. Water (1500 ml) was added while stirring. Then, 2-propanone (100 ml) was added dropwise under slight cooling. The mixture was decomposed with HCl (180 ml). The organic layer was separated, dried, filtered and the solvent evaporated, yielding 295 g of (-)-(R)-3,4-dihydro-2H-1-benzopyran-2-methanol (interm. 3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06133277 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-ae668af34f7245bf9cf7d74adb418c83 |
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| Source note | uspto-grants-2000_10 |
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