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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179359Generated: October 30, 2026

Borane;tetrahydrofuran → HCID 68109324, compound

https://huagongshe.com/reaction/2179359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBorane;tetrahydrofuranHCID 2723981—
Reactant8-bromo-2,3,4,5-tetrahydro-1H-benzofuro[3,2-c]azepin-1-oneHCID 68108459—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68109324HCID 6810932445.3%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a slurry of the product of step C (858 mg, 3.06 mmol) in anhydrous THF (6 mL) was added 1 M borane-THF complex (1 N in THF, 15.3 mL, 15.3 mmol) at ambient temperature. The reaction mixture was heated to 65° C. for 15 h. After cooling to ambient temperature, the reaction mixture was quenched with 1 M HCl and concentrated in vacuo. The residue was basified with 1 M NaOH and extracted with dichloromethane. The organic layer was dried over sodium sulfate, filtered, and concentrated in vacuo to give the crude material which was purified by flash column chromatography (SiO2, 90:10 dichloromethane/methanol) to provide 8-bromo-2,3,4,5-tetrahydro-1H-benzofuro[3,2-c]azepine (369 mg, 45%) as a pale yellow solid: 1H NMR (CDCl3, 300 MHz) δ 7.53 (d, J=1.8 Hz, 1H), 7.33-7.28 (m, 1H), 7.21 (d, J=8.4 Hz, 1H), 3.95 (s, 2H), 3.18 (td, J=3.9, 2.4 Hz, 2H), 3.00 (t, J=6.0 Hz, 2H), 1.94-1.84 (m, 2H), 1.57 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067949B2
Source datasetuspto-grants-2015_06
ORD IDord-cf07bfbebc5c43eea42a66ee723cbf46
Source noteuspto-grants-2015_06