HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264171Generated: November 1, 2026
Sodium Bicarbonate → HCID 60124979, compound
https://huagongshe.com/reaction/2264171
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-Bromo-6,7,8,9-tetrahydro-5H-benzo[7]annulen-5-one | HCID 10610018 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 60124979 | HCID 60124979 | — |
Reaction Steps
To a stirred solution of 1.91 g (8.0 mmol) of 3-bromo-6,7,8,9-tetrahydro-5H-benzo[7]annulen-5-one (J. Med. Chem. 2000, 43, 2049-2063) in 40 mL of ethanol under nitrogen cooled in an ice-bath was added 0.635 g (16.8 mmol, 2.1 equiv) of sodium borohydride. After three hours 32 mL of saturated sodium bicarbonate solution was added, and the mixture was concentrated under reduced pressure to remove the ethanol. The aqueous residue was diluted with 8 mL water and extracted with 2×80 mL of ethyl acetate. The combined extract was washed with 10 mL each of water and brine, dried over sodium sulfate, filtered, and concentrated to give product as a white crystalline solid. MS (m+1)=242.2; 1H NMR (400 MHz, CDCl3) 7.62 (s, 1H), 7.25 (m, 1H), 6.95 (d, 1H, J 8 Hz), 4.89 (d, 1H, J 9 Hz), 2.84 (m, 1H), 2.65 (d, 1H, J 12 Hz), 1.99 (m, 2H), 1.78 (m, 4H), 1.38 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07855201B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-5faee6943e0246cca595c7eb151399c4 |
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| Source note | uspto-grants-2010_12 |
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