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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1806193Generated: November 1, 2026

Indoline → tert-Butyl indoline-1-carboxylate

https://huagongshe.com/reaction/1806193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndolineHCID 10328—
ReactantCarbonic acid, bis(1,1-dimethylethyl) esterHCID 10219638—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl indoline-1-carboxylateHCID 366395482%

Reaction Steps

Indoline (10 g, 84 mmol) was dissolved in tetrahydrofuran (100 mL) and di-tert-butylcarbonate (22 g, 0.1 mol) was added. The mixture was left stirring for 16 hours at room temperature under an inert nitrogen atmosphere. The tetrahydrofuran was removed in vacuo and the crude product purified by vacuum distillation to give the title compound (15.1 g) as a clear pale pink oil that crystallised upon standing (temperature: 160-162° C., pressure 1-0.1 mm Hg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354406B2
Source datasetuspto-grants-2013_01
ORD IDord-6a0bd64bc6314056991bfc49f5a70e18
Source noteuspto-grants-2013_01