HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168028Generated: October 25, 2026
Sodium Chloride → methyl N-[3-(3,4-dichlorophenyl)benzyl]carbamate
https://huagongshe.com/reaction/1168028
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Methyl (3-bromobenzyl)carbamate | HCID 12090302 | — |
| Reactant | 3,4-Dichloro-phenyl-boric acid | HCID 21939927 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | methyl N-[3-(3,4-dichlorophenyl)benzyl]carbamate | HCID 12090301 | 94.8% |
Reaction Steps
1.30 g of methyl N-(3-bromobenzyl)carbamate, 0.56 g of sodium carbonate in aqueous solution (20 ml) and 0.13 g of tetrakis(triphenylphosphine)palladium (0) were added to toluene (40 ml) under a nitrogen atmosphere. The resulting solution was mixed with 1.02 g of 3,4-dichlorophenylboric acid in ethanol (20 ml) at room temperature with stirring and refluxed under heating for 2 hours. After the reaction, the reaction solution was cooled to room temperature, poured into saturated aqueous sodium chloride and extracted with ethyl acetate, and the organic layer was dried over anhydrous magnesium sulfate and evaporated under reduced pressure for removal of the solvent. The residue was purified by silica gel column chromatography to give 1.45 g of methyl N-[3-(3,4-dichlorophenyl)benzyl]carbamate as a yellow transparent viscous liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06620961B1 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-3e5923a69dfd4da18e8f75f5ae234dfe |
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| Source note | uspto-grants-2003_09 |
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