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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556451Generated: October 29, 2026

Water → Rac-6-chloro-3-(4-chloro-benzyl)-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/556451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantZ-6-chloro-3-(4-chloro-benzylidene)-1,3-dihydro-indol-2-oneHCID 962924—
ReactantSodium borohydrideHCID 4311764—
SolventDimethyl SulfoxideHCID 679—
SolventMethanolHCID 887—
ProductRac-6-chloro-3-(4-chloro-benzyl)-1,3-dihydro-indol-2-oneHCID 5750729794.9%

Reaction Steps

Sodium borohydride (3.0 g, 79 mmol) (Aldrich) was added in small portions to a suspension of 6-chloro-3-(4-chloro-benzylidene)-1,3-dihydro-indol-2-one (19 g, 66 mmol) (from example 76a supra) in methanol (200 mL) and DMSO (50 mL) at such a rate that gas evolution was not too vigorous. When the addition was complete, mixture was stirred at room temperature for 0.5 h-1 h. After water (200 mL) was added, the resulting precipitate was collected and dried to give 18.3 g of rac-6-chloro-3-(4-chloro-benzyl)-1,3-dihydro-indol-2-one as a light yellow solid. MS: 293 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058269B2
Source datasetuspto-grants-2011_11
ORD IDord-e584bd647ca54cc4981c54b738a5fb17
Source noteuspto-grants-2011_11