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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387303Generated: October 30, 2026

Carbon Dioxide → 1h-Indole-1,7-dicarboxylic acid,6-fluoro-2,3-dihydro-,1-(1,1-dimethylethyl)ester

https://huagongshe.com/reaction/387303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantTert-butyl 6-fluoroindoline-1-carboxylateHCID 17985580—
ReactantCID 53628100HCID 178418400—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product1h-Indole-1,7-dicarboxylic acid,6-fluoro-2,3-dihydro-,1-(1,1-dimethylethyl)esterHCID 5933264577%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred solution of 1,1-dimethylethyl 6-fluoro-2,3-dihydro-1H-indole-1-carboxylate (8.7 g, 0.037 mol) in Et2O (150 mL) at −78° C. was added TMEDA (7.2 mL, 0.048 mol) and a solution of 1M sec-BuLi (44 mL, 0.044 mol) dropwise. The reaction mixture was stirred for 1 h at −78° C. and then poured onto crushed CO2 (250 mL). The mixture was allowed to warm to room temperature overnight. The suspension was diluted with water (200 mL) and diethyl ether (50 mL), and the layers were separated. The aqueous fraction was acidified with 1M HCl and extracted with diethyl ether (3×100 mL). The combined organic layers were washed with brine (1×50 mL), dried (Na2SO4), and concentrated under reduced pressure giving 8.0 g (77%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372875B2
Source datasetuspto-grants-2013_02
ORD IDord-12ad61ce5ac04d818d4a51b5a1fe53f6
Source noteuspto-grants-2013_02