Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387240Generated: October 27, 2026

Indoline → tert-Butyl indoline-1-carboxylate

https://huagongshe.com/reaction/387240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndolineHCID 10328—
ReactantSodium HydroxideHCID 14798—
ReactantCarbonic acid, bis(1,1-dimethylethyl) esterHCID 10219638—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Producttert-Butyl indoline-1-carboxylateHCID 366395483%

Reaction Steps

A solution of di-tert-butylcarbonate (427.1 g, 1.96 mol) in CH2Cl2 (500 mL) was added dropwise at room temperature to a solution of indoline (212 g 1.78 mol) in CH2Cl2 (1000 mL). A solution of NaOH (85.3 g, 2.13 mol) in water (500 mL) was then added dropwise and the mixture was stirred overnight. The layers were separated and the organic layer was washed with 5% NaOH, brine and dried over Na2SO4. The organic layer was concentrated under reduced pressure and the crude product was crystallized with petroleum ether, giving 324 g (68%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372875B2
Source datasetuspto-grants-2013_02
ORD IDord-5c64f8a4d0c54af5967e7160b91af836
Source noteuspto-grants-2013_02