Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102677Generated: October 31, 2026

Sodium borohydride → HCID 57803061, compound

https://huagongshe.com/reaction/2102677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57803050HCID 57803050—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 57803061HCID 57803061—

Reaction Conditions

Temperature40 °C

Reaction Steps

Sodium borohydride (0.38 g, 10 mmol) (Aldrich) was added in small portions to a solution of 4-(6-chloro-2-oxo-1,2-dihydro-indol-3-ylidene)-piperidine-1-carboxylic acid tert-butyl ester (0.35 g, 1 mmol) (from Example 12a supra) in methanol (25 mL) and water (3 mL) at such a rate that gas evolution was not too vigorous. When addition was complete, mixture was heated at 40° C. for 1 hour. After cooling, mixture was slowly diluted with water. Precipitate formed was collected by filtration and washed with cold aqueous methanol to give rac-4-(6-chloro-2-oxo-2,3-dihydro-1H-indol-3-yl)-piperidine-1-carboxylic acid tert-butyl ester as a white crystalline material. (Yield 0.33 g, 94.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576082B2
Source datasetuspto-grants-2009_08
ORD IDord-a65d9e0485ee4997a9e235521b22aeff
Source noteuspto-grants-2009_08