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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389533Generated: October 31, 2026

2,4-Difluorobenzaldehyde → HCID 59400138, compound

https://huagongshe.com/reaction/2389533

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DifluorobenzaldehydeHCID 73770—
ReactantBoc-3-amino-1,2,3,4-tetrahydroquinolineHCID 4460996—
ReactantTetramethylammonium Triacetoxyborohydride (>90%)HCID 13696215—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 59400138HCID 5940013897.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of tert-butyl 1,2,3,4-tetrahydroquinolin-3-ylcarbamate (248 mg, 1.0 mmol) and 2,4-difluorobenzaldehyde (300 mg, 2.11 mmol) in 1,2-dichloroethane (10 mL) was added tetramethylammonium triacetoxyborohydride (0.6 g, 2.0 mmol). The mixture was stirred at 50° C. for 20 hours. The mixture was quenched by addition of saturated Rochelle's salt (10 mL) and extracted with dichloromethane (3×10 mL). The combined organic layers were washed with water (2×10 mL), dried over anhydrous sodium sulfate and evaporated to dryness. The residue was purified by chromatography on silica gel (5-40% EtOAc/Hexane) to give tert-butyl 1-(2,4-difluorobenzyl)-1,2,3,4-tetrahydroquinolin-3-ylcarbamate (365 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273754B2
Source datasetuspto-grants-2012_09
ORD IDord-c45f8df28ee245cfac8ffe1129365fe4
Source noteuspto-grants-2012_09