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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 468402Generated: October 29, 2026

Water → 5-Ethyl-1-(phenylsulfonyl)indoline

https://huagongshe.com/reaction/468402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantSodium borohydrideHCID 4311764—
Reactant1-(1-Benzenesulfonyl-2,3-dihydro-1H-indol-5-yl)-ethanoneHCID 14112956—
SolventTrifluoroacetic acidHCID 6422—
Product5-Ethyl-1-(phenylsulfonyl)indolineHCID 1411295247%

Reaction Conditions

Temperature25 °C

Reaction Steps

To TFA (1600 mL) at 0° C. was added sodium borohydride (64.0 g, 1.69 mol) over 1 h. To this mixture was added dropwise a solution of 1-(1-(phenylsulfonyl)indolin-5-yl)ethanone (40.0 g, 0.133 mol) in TFA (700 mL) over 1 h. The mixture was then stirred overnight at 25° C. After dilution with H2O (1600 mL), the mixture was made basic by the addition of sodium hydroxide pellets at 0° C. The organic layer was separated and the aqueous layer was extracted with CH2Cl2. The combined organic layers were washed with brine, dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by silica column to give 5-ethyl-1-(phenylsulfonyl)indoline (16.2 g, 47% over two steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623905B2
Source datasetuspto-grants-2014_01
ORD IDord-77453fad533f4f1cbc3f6b7594267c47
Source noteuspto-grants-2014_01