Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857074Generated: October 31, 2026

Isopropanol → 1-Methylethyl 2-methoxyacetate

https://huagongshe.com/reaction/1857074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantMethyl chloroacetateHCID 7295—
ReactantChlorineHCID 24526—
ReactantSodium MethoxideHCID 10942334—
SolventWaterHCID 962—
Product1-Methylethyl 2-methoxyacetateHCID 54219277%

Reaction Conditions

Temperature25 °C

Reaction Steps

434.1 g (4.0 mol) of methyl chloroacetate are initially introduced and stirred at 25° C. 756.3 g (4.2 mol) of 30% strength sodium methoxide solution are added dropwise in the course of 2.5 h such that a reaction temperature of 65° C. is not exceeded. After the addition, stirring is continued at reflux temperature for a further 3 h. 407.5 g of methanol are then separated from the reaction mixture by distillation. 480.8 g (8 mol) of isopropanol are added to the residue and the mixture is heated under reflux. In the course of this, methanol is removed through a 0.5 m long Multifil column at a reflux ratio of approximately 1:1 (291.9 g of distillate). After 6.5 h, the conversion of the methyl methoxyacetate to the isopropyl methoxyacetate is >98%. After cooling, the reaction mixture is filtered off with suction and the residue is washed with 450 g of isopropanol. A residue of 412.1 g and a liquid phase (filtrate and wash liquid) of 969.9 g are obtained. The liquid phase is fractionated through a 0.5 m long Multifil column. Isopropyl methoxyacetate (405.0 g, yield 77%) with an organic purity of >99%, a chlorine content of 10 ppm and a water content of <0.05% is obtained as the main fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06143920
Source datasetuspto-grants-2000_11
ORD IDord-830697164340421fa8ea6ff82b6bb81e
Source noteuspto-grants-2000_11