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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83986Generated: October 25, 2026

Sodium bis(2-methoxyethoxy)aluminiumhydride → 5-Chloro-1'-[trans-3-(4-chlorophenyl)allyl]spiro[indoline-3,3'-pyrrolidine]

https://huagongshe.com/reaction/83986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium bis(2-methoxyethoxy)aluminiumhydrideHCID 21584525—
Reactant1-Methanesulfonyl-5-chloro-1'-[trans-3-(4-chlorophenyl)allyl]spiro[indoline-3,3'-pyrrolidine]HCID 68924239—
SolventTolueneHCID 1140—
Product5-Chloro-1'-[trans-3-(4-chlorophenyl)allyl]spiro[indoline-3,3'-pyrrolidine]HCID 6893064974.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 1-methanesulfonyl-5-chloro-1′-[trans-3-(4-chlorophenyl)allyl]spiro[indoline-3,3′-pyrrolidine] obtained in Step D (256 mg) in toluene (25 ml) under argon was treated with sodium bis(2-methoxyethoxy)aluminium hydride (Red-Al, 65% in toluene, 0.67 ml) and the reaction mixture was stirred at 100° C. for 1 hour, cooled to room temperature, quenched by addition of ethyl acetate (10 ml), stirred for 15 min and concentrated in vacuo. The residue was purified by silica gel chromatography (eluent ethyl acetate:methanol 95:5) to afford 5-chloro-1′-[trans-3-(4-chlorophenyl)allyl]spiro[indoline-3,3′-pyrrolidine] (157 mg) as a yellow oil, which was characterised by its mass and NMR spectra.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846907B2
Source datasetuspto-grants-2014_09
ORD IDord-8798f0c9457348929512f941c499cc49
Source noteuspto-grants-2014_09