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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764794Generated: November 2, 2026

Sodium Hydroxide → HCID 22036736, compound

https://huagongshe.com/reaction/1764794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantRed-AlHCID 16684438—
Reactant7-Fluoro-2,3,4,5-tetrahydro-1,5-benzothiazepin-4-oneHCID 22036759—
SolventTolueneHCID 1140—
ProductHCID 22036736HCID 2203673693%

Reaction Conditions

Temperature0 °C

Reaction Steps

7-fluoro-2,3-dihydro-1,5-benzothiazepin-4(5H)-one (76 mg, 0.38 mmol) dissolved in toluene (1 mL) and cooled to 0° C. in an ice bath. Red-Al (275 mL, 0.91mmol) was added and then the reaction allowed to warm to room temperature. The reaction was heated at reflux for 1.5 hours. 1 N sodium hydroxide was added slowly until pH>10, this was stirred for 10 minutes, extracted with dichloromethane (3×25 mL), washed with water, and dried (sodium sulfate). The concentrated organics were purified by preparative thin layer chromatography on silica gel and eluted with 50% ethyl acetate in hexanes to give 7-fluoro-2,3,4,5-tetrahydro-1,5-benzothiazepine (30.8 mg, 93%). 1H NMR (CDCl3, 300 MHz): δ 7.32 (t, 1H, J=7.5 Hz), 6.53-6.42 (m, 2H), 4.09 (s-broad, 1H), 3.31-3.27 (m, 2H), 2.83-2.79 (m, 2H), 2.11-2.04 (m, 2H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE039680E1
Source datasetuspto-grants-2007_06
ORD IDord-ea2841c03dfc45ac9ae0973040dc1a65
Source noteuspto-grants-2007_06