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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1460487Generated: October 31, 2026

Sodium bis(2-methoxyethoxy)aluminiumhydride → (S)-5,11-Dihydro-5-(2-pyrrolidinylmethyl)dibenzo[b,e][1,4]-thiazepine

https://huagongshe.com/reaction/1460487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium bis(2-methoxyethoxy)aluminiumhydrideHCID 21584525—
Reactant(S)-5,11-Dihydro-5-(1-[4-methylphenylsulphonyl]-2-pyrrolidinylmethyl)dibenzo[b,e][1,4]thiazepineHCID 22841645—
SolventTolueneHCID 1140—
Product(S)-5,11-Dihydro-5-(2-pyrrolidinylmethyl)dibenzo[b,e][1,4]-thiazepineHCID 2284164755.1%

Reaction Steps

Sodium bis(2-methoxyethoxy)aluminium hydride ("Red-Al"-registered Trade Mark) (20.8 ml of a 3.4M solution in toluene) was added to a solution of (S)-5,11-dihydro-5-(1-[4-methylphenylsulphonyl]-2-pyrrolidinylmethyl)dibenzo[b,e][1,4]thiazepine (see Preparations 15 and 16) (8.0 g) in toluene (50 ml) and the mixture heated under reflux for 27 hours, allowed to cool to room temperature, quenched by the addition of 2.5M aqueous sodium hydroxide solution, diluted with water and extracted with ethyl acetate. The combined organic extracts were washed with saturated aqueous sodium chloride solution, dried over sodium sulphate and evaporated under reduced pressure. The residue was purified by chromatography on silica gel, performing a gradient elution initially using dichloromethane as eluant and changing to dichloromethane/saturated methanolic ammonia (90:10). Appropriate fractions were combined and evaporated under reduced pressure to give the title compound as a colourless oil, (2.9 g, 55%), [α]589 -4.9° (c=1.065 in ethanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05071844
Source datasetuspto-grants-1991_12
ORD IDord-38e002976d0d408f98629c5d4ce871c2
Source noteuspto-grants-1991_12