Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105282Generated: November 1, 2026

Bromomethyl methyl ether → HCID 66717624, compound

https://huagongshe.com/reaction/2105282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromomethyl methyl etherHCID 83093—
ReactantHCID 3726134HCID 3726134—
SolventDichloromethaneHCID 6344—
SolventDiisopropylethylamineHCID 81531—
ProductHCID 66717624HCID 66717624—

Reaction Conditions

Temperature0 °C

Reaction Steps

The Sulfonamide of Step One, 3-phenylsulfamoylthiophene-2-carboxyli-c acid methyl ester, was dissolved in dry dichloromethane and N,N-diisopropyl ethylamine. The resulting mixture was chilled to 0° C. prior to the addition of bromomethyl methyl ether. The reaction mixture was stirred over night at room temperature. The mixture was partitioned between dichloromethane and aqueous HCl (2N). The organic layer will then be washed one time with saturated sodium chloride solution and dried over sodium sulfate, followed by concentration to dryness under reduced pressure to give the desired product, 3-(N-methoxymethyl-N-phenylsulfamoyl)thiophene-2-carboxylic acid methyl ester (3 g, quantitative).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579340B2
Source datasetuspto-grants-2009_08
ORD IDord-b5eb34c61c094a518c4de5e42f4d4fad
Source noteuspto-grants-2009_08