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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 85115Generated: October 27, 2026

Salicylaldehyde → Tert-butyl 3-(2-formylphenoxy)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/85115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylaldehydeHCID 6998—
ReactantPotassium CarbonateHCID 11430—
ReactantTert-butyl 3-(methanesulfonyloxy)pyrrolidine-1-carboxylateHCID 4139999—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 3-(2-formylphenoxy)pyrrolidine-1-carboxylateHCID 5827899423.7%

Reaction Steps

2-Hydroxybenzaldehyde (25; 1.2 g, 9.8 mmol), N-Boc-3-(methylsulfonyloxy)pyrrolidine (29; 2.6 g, 9.8 mmol), K2CO3 (2.0 g, 14.7 mmol) and tetrabutyl ammonium iodide (300 mg, cat) in CH2Cl2 (20 mL) was stirred at 70-80° C. for 18 h. DMF was removed by concentration under reduced pressure. The resulting residue was diluted with EtOAc (100 mL), washed with water (50 mL), dried (MgSO4) and concentrated under reduced pressure. The resulting residue was purified by chromatography (pentane:EtOAc=1:10) to afford 676 mg of tert-butyl 3-(2-formylphenoxy)pyrrolidine-1-carboxylate 30 as an oil (yield: 23%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846947B2
Source datasetuspto-grants-2014_09
ORD IDord-e8ac84473b154dedbd0a13d496ecee4e
Source noteuspto-grants-2014_09