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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644810Generated: October 31, 2026

3-Chloroaniline → HCID 66774596, compound

https://huagongshe.com/reaction/1644810

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ChloroanilineHCID 7932—
ReactantSodium borohydrideHCID 4311764—
Reactant1,1-Dimethylethyl (2S)-4,4-difluoro-2-formyl-1-pyrrolidinecarboxylateHCID 86635622—
SolventMethanolHCID 887—
SolventTitanium isopropoxideHCID 11026—
ProductHCID 66774596HCID 6677459612%

Reaction Steps

Solution of (S)-4,4-difluoro-2-formyl-pyrrolidine-1-carboxylic acid tert-butyl ester (1 g, 0.0042 mol) and 3-chloroaniline (0.53 mL, 0.0042 mol) in titanium tetraisopropoxide (5 mL) was allowed to stir for 12 h. The reaction was monitored by TLC. After disappearance of starting reaction on TLC, the mixture was diluted with methanol (20 mL) followed by the addition of sodium borohydride (0.33 g, 0.0084 mol) in portions. The reaction mixture was stirred for 6 h. The reaction was quenched with water and extracted with DCM (3×50 mL). The organic layer was dried over anhydrous Na2SO4 and the volatiles were removed using a rotary evaporator to give a crude oil, which was then purified via column chromatography (5% methanol: DCM, mesh Size—100-200 silica, diameter of column—2.5 cm, height of silica—approx. 4 inch) to afford the desired (S)-2-[(3-chloro-phenylamino)-methyl]-4,4-difluoro-pyrrolidine-1-carboxylic acid tert-butyl ester as a sticky solid (0.15 g, 12%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124636B2
Source datasetuspto-grants-2012_02
ORD IDord-ca58ea44ad44491c918b1f93ba753e6b
Source noteuspto-grants-2012_02