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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793541Generated: November 2, 2026

Potassium Sodium Tartrate → 2,3,4,5-tetrahydro-1H-1-benzazepine

https://huagongshe.com/reaction/1793541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Sodium TartrateHCID 9357—
Reactant1,3,4,5-Tetrahydro-2H-1-benzazepin-2-oneHCID 248580—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product2,3,4,5-tetrahydro-1H-1-benzazepineHCID 57650398%

Reaction Steps

A solution of 1,3,4,5-tetrahydro-2H-1-benzazepin-2-one (2.71 g, 16.7 mmol) in THF (40 mL) was added dropwise to a suspension of LAH (1.27 g, 33.4 mmol) in ether (150 mL) at room temperature. The mixture was refluxed for 16 h. Saturated Rochelle's salt solution (15 mL) was added to the mixture cooled with an ice-water bath. The mixture was stirred for 2 hrs and the two layers were separated. The aqueous layer was extracted with ether (2×25 mL). The combined organic layer was dried (Na2SO4), concentrated in vacuo and flash column chromatography (EtOAc:hexane/3:7) gave 2,3,4,5-tetrahydro-1H-1-benzazepine (2.40 g, 98%) as a yellow liquid. 1H NMR (CDCl3, 300 MHz) δ 1.58–1.70 (m, 2H), 1.72–1.86 (m, 2H), 2.72–2.82 (m, 2H), 3.00–3.10 (m, 2H), 3.78 (br, 1H), 6.74 (dd, J=1.1, 7.7 Hz, 1H), 6.82 (td, J=7.3, 1.1 Hz, 1H), 7.04 (td, J=7.5, 1.5 Hz, 1H), 7.11(d, J=7.4 Hz, 1H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07081455B2
Source datasetuspto-grants-2006_07
ORD IDord-6e01e8843e3e4e8cb5ca3e3fd9f2faca
Source noteuspto-grants-2006_07