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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363087Generated: October 29, 2026

Acetic Acid → tert-Butyl 1-benzyl-6-chloro-1,2,3,4-tetrahydroquinolin-3-ylcarbamate

https://huagongshe.com/reaction/1363087

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzaldehydeHCID 240—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl 6-chloro-1,2,3,4-tetrahydroquinolin-3-ylcarbamateHCID 59297067—
Solvent1,2-DichloroethaneHCID 11—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl 1-benzyl-6-chloro-1,2,3,4-tetrahydroquinolin-3-ylcarbamateHCID 5929704980%

Reaction Steps

To a solution of 21A (310 mg, 1.096 mmol) in 1,2-dichloroethane (7 mL) was added benzaldehyde (235 mg, 2.193 mmol), followed by sodium triacetoxyborohydride (650 mg, 3.069 mmol) and AcOH (200 mg, 3.29 mmol). The reaction mixture was stirred at RT for 4 h, then diluted with EtOAc, washed with saturated aqueous NaHCO3, water, brine, dried Na2SO4) and concentrated. The resulting residue was chromatographed (silica gel) eluting with EtOAc/hexane 1:5 to give the title compound as light yellow foam (325 mg, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884113B2
Source datasetuspto-grants-2011_02
ORD IDord-8042fda8d02d4cef93e44220a3407d03
Source noteuspto-grants-2011_02