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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437517Generated: November 2, 2026

6-Bromo-2,3,4,9-tetrahydro-1H-carbazol-1-one → HCID 597396, compound

https://huagongshe.com/reaction/1437517

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-2,3,4,9-tetrahydro-1H-carbazol-1-oneHCID 708529—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductHCID 597396HCID 59739650.4%

Reaction Steps

To a solution of 6-bromo-2,3,4,9-tetrahydro-1H-carbazol-1-one (500 mg, 1.9 mmol) in methanol (20 mL) was added sodium borohydride (144 mg, 3.8 mmol) portionwise. The reaction mixture was stirred for one hour and quenched with water (5 mL). The reaction was concentrated, diluted with methylene chloride, and washed with water. The organic phase was concentrated and the crude alcohol purified by flash chromatography on silica (5% to 30% ethyl acetate/hexanes gradient) to provide 6-bromo-2,3,4,9-tetrahydro-1H-carbazol-1-ol (255 mg, 50%). as a light brown solid. 1H-NMR (DMSO-d6): δ 10.99 (s, 1H), 7.54 (d, 1H), 7.25 (d, 1H), 7.12 (dd, 1H), 5.18 (d, 1H), 4.75-4.70 (m, 1H), 2.64-2.53 (m, 2H), 2.02-1.91 (m, 2H), 1.77-1.66 (m, 2H); MS m/z (M+1) 267.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622494B2
Source datasetuspto-grants-2009_11
ORD IDord-f2f59b3d99354c8896118491dc580e2e
Source noteuspto-grants-2009_11