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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651655Generated: November 1, 2026

1-(Chloromethoxy)-2-methoxyethane → HCID 14700405, compound

https://huagongshe.com/reaction/1651655

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Chloromethoxy)-2-methoxyethaneHCID 77590—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 23050267HCID 23050267—
SolventDichloromethaneHCID 6344—
ProductHCID 14700405HCID 1470040566%

Reaction Steps

A solution of 2-bromo-3-(l-hydroxyethyl)thiophene (97.5 g, 0.47 mol) in dry methylene chloride (400 ml) was cooled in ice and N,N-diisopropylethylamine (68.2 g, 0.517 mol) was added followed by methoxyethoxymethYl chloride (64.4 g, 0.517 mol). The solution was stirred at room temperature over night. The dark solution was washed with water, 3N HCl, saturated NaHCO3 and finally with water. The solution was dried over anhydrous Na2SO4 filtered and concentrated in vacuo at room temperature. A dark amber oil was obtained (123.1 g). The impure product was distilled and the product was collected at 108-116° C. at 0.7 mm Hg. to give 91.1 g (66%) of colorless liquid. NMR supported the structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04929637
Source datasetuspto-grants-1990_05
ORD IDord-bf5ef5f878414079ae6ce26899adc3be
Source noteuspto-grants-1990_05