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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45991Generated: October 26, 2026

Indoline-2-carboxylic acid, (S)- → (S)-(+)-2-Indolinemethanol

https://huagongshe.com/reaction/45991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoline-2-carboxylic acid, (S)-HCID 2733920—
SolventTetrahydrofuranHCID 8028—
Product(S)-(+)-2-IndolinemethanolHCID 695118687%

Reaction Steps

To a solution of (S)-indoline-2-carboxylic acid (9.2 mmol, 1.0 equiv.) in THF (18 ml) was added dropwise BH3-DMS solution (18.4 mmol, 2 equiv.) and the reaction mixture was heated to reflux for 12 h. The mixture was quenched with methanol (7.5 ml) and conc. HCl (2.5 ml) with cooling and was then refluxed for additional 2 h. The solvent was evaporated and the residue was basified with 40% NaOH solution and extracted with dichloromethane. The organic layer was washed with brine, dried over sodium sulfate and the solvent was evaporated under reduced pressure to give the crude product which was purified by silica gel column chromatography. Yield: 87%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541573B2
Source datasetuspto-grants-2013_09
ORD IDord-5980e20ebdce4253b889a339eb09cf2f
Source noteuspto-grants-2013_09