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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862246Generated: November 2, 2026

Dichloromethane → 3-Acetoxy-2-(methoxycarbonyl)methoxypyridine

https://huagongshe.com/reaction/1862246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantBoron trifluoride etherateHCID 8000—
ReactantTert-Butyl nitriteHCID 10906—
Reactant3-Amino-2-(methoxycarbonyl)methoxypyridineHCID 12115512—
SolventAcetic AnhydrideHCID 7918—
SolventPentaneHCID 8003—
Solvent1,2-DimethoxyethaneHCID 8071—
Product3-Acetoxy-2-(methoxycarbonyl)methoxypyridineHCID 1211551336.4%

Reaction Steps

1.6 g of boron trifluoride diethyl etherate was added to a mixture of 1.0 g of 3-amino-2-(methoxycarbonyl)methoxypyridine, 3 ml of 1,2-dimethoxyethane and 1 ml of dichloromethane dropwise at −10° C. The mixture was stirred for 10 minutes at the same temperature, then, to the reaction solution was added a solution of 0.68 g of t-butyl nitrite in 1 ml of 1,2-dimethoxyethane dropwise at −5° C. or lower. The mixture was stirred for 30 minutes at the same temperature, then, into the mixture was poured n-pentane. The lower layer of two separated layers was dissolved in 5 ml of acetic anhydride, and the mixture was stirred for 1 hour at 80° C. The solvent was distilled off, then, the resulted residue was subjected to silica gel chromatography to obtain 0.45 g of 3-acetoxy-2-(methoxycarbonyl)methoxypyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06537948B1
Source datasetuspto-grants-2003_03
ORD IDord-4940deffccc8447e857ef24154566f87
Source noteuspto-grants-2003_03