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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044477Generated: October 26, 2026

Pyrrolidine → HCID 57467187, compound

https://huagongshe.com/reaction/1044477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
Reactant7-Methoxy-2-tetraloneHCID 77785—
Reactant4-(Bromomethyl)-1,2-dichlorobenzeneHCID 639726—
ReactantDichloromethane methanol waterHCID 21958822—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
ProductHCID 57467187HCID 5746718784.4%

Reaction Steps

15 g (85 mmol) of 7-methoxy-3,4-dihydronaphthalen-2(1H)-one were dissolved in 200 ml of dry MeOH under nitrogen. Then 6.66 g (94 mmol) of pyrrolidine were added dropwise and slowly and the colour changes. The mixture is stirred for one h. The solvent was reduced under vacuo and the residue was dissolved in MeCN. At 5° C. 22.5 g (94 mmol) 4-(bromomethyl)-1,2-dichlorobenzene dissolved in MeCN were added and the mixture was stirred over night at RT. The solvent was reduced under vacuo and the residue was mixed with MeOH/CH2Cl2/H2O 1:1:1 (50 ml, 50 ml, 50 ml) and 10 ml of glacial acid were added. The mixture was stirred over night. Work-up: The reaction mixture was put on ice water and extracted 3× with CH2Cl2. The combined organic layers were washed 1× with NaHCO3 solution and 1× with saturated NaCl solution. The organic phase was dried on MgSO4 and the solvent was evaporated. The residue (31.5 g) was purified by flash-chromatography on silica gel with heptane/EtOAc 2:1. 24.1 g (71.7 mmol, 84%) of the product were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563617B2
Source datasetuspto-grants-2013_10
ORD IDord-5e856d25e79f4acdab3204c173b51c94
Source noteuspto-grants-2013_10