HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296107Generated: October 30, 2026
Sodium borohydride → HCID 58909483, compound
https://huagongshe.com/reaction/1296107
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-Bromo-1H-2-benzopyran-4(3H)-one | HCID 45489802 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58909483 | HCID 58909483 | 95.8% |
Reaction Steps
A solution of sodium borohydride (300 mg, 7.93 mmol) dissolved in a minimum amount of ice cold water was added dropwise at 0° C. to a solution of 6-Bromo-isochroman-4-one (1.49 g, 6.56 mmol) in absolute ethanol (27.0 mL). The reaction mixture was stirred at room temperature for 2 h. The reaction mixture was partitioned between ethyl acetate and saturated sodium bicarbonate solution. The phases were separated and the organic phase washed with water and saturated sodium chloride, dried (sodium sulfate), filtered, and concentrated under reduced pressure to yield 6-Bromo-isochroman-4-ol (1.44 g, 95%) as a white solid: 1H NMR (300 MHz, CDCl3) δ 7.40 (dd, J=8.3, 1.8 Hz, 1H), 7.30 (d, J=8.3 Hz, 1H), 7.15 (d, J=1.8 Hz, 1H), 4.63 (ABq, J=15.3 Hz, 2H), 4.49 (d, J=8.6 Hz, 1H), 4.07 (dd, J=12.0, 2.8 Hz, 1H), 3.83 (dd, J=12.0, 2.8 Hz, 1H), 2.60 (d, J=9.2 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07244725B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-ff5ca39a2d734665aa419d1698a0632d |
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| Source note | uspto-grants-2007_07 |
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