HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182259Generated: October 31, 2026
Bromomethyl methyl ether → HCID 66717624, compound
https://huagongshe.com/reaction/1182259
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromomethyl methyl ether | HCID 83093 | — |
| Reactant | HCID 3726134 | HCID 3726134 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Diisopropylethylamine | HCID 81531 | — |
| Product | HCID 66717624 | HCID 66717624 | — |
Reaction Steps
The Sulfonamide of Step One, 3-phenylsulfamoylthiophene-2-carboxylic 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07288538B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-418c79901dbc415fb97865a5bbd1e063 |
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| Source note | uspto-grants-2007_10 |
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