Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505656Generated: October 30, 2026

Ammonium Chloride → Methyl 2-azido-3-(2-methoxy-3-methylphenyl)acrylate

https://huagongshe.com/reaction/1505656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2,4-Dimethoxy-3-methylbenzaldehydeHCID 251693—
ReactantMethyl 2-azidoacetateHCID 4020482—
ReactantHCID 178418582HCID 178418582—
SolventMethanolHCID 887—
ProductMethyl 2-azido-3-(2-methoxy-3-methylphenyl)acrylateHCID 9040554488.5%

Reaction Steps

To the mixture of 2.46 g of 2-methoxy-3-methylanisaldehyde (16 mmol) and 4.72 g of methyl azidoacetate (41 mmol) in 20 mL of MeOH is added 7.6 mL of 5.4M MeONa over 30 minute at −10 degrees. After addition the mixture was stirred for additional hour at the same temperature and then transferred in cold room (4 degrees) and stirred overnight. On the morning reaction mixture was poured in 0.5 L mixture of ice and conc. ammonium chloride solution, stirred for 10 minutes and filtered off. The solid was washed with plenty of ice cold water and then moved at ambient temperature. After air drying for 1 hr the solid was dissolved in 50 mL of DCM, dried over magnesium sulfate and passed through short silica gel plug. Evaporation of solvent produced 3.5 g of methyl 2-azido-3-(2-methoxy-3-methylphenyl)acrylate, that was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216993B2
Source datasetuspto-grants-2015_12
ORD IDord-d0ee719e5025401f921542c170ec674e
Source noteuspto-grants-2015_12