HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168029Generated: October 26, 2026
Sodium Chloride → isopropyl N-(3-phenylbenzyl)carbamate
https://huagongshe.com/reaction/1168029
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Phenyl dihydrogen orthoborate | HCID 78412 | — |
| Reactant | isopropyl N-(3-bromobenzyl)carbamate | HCID 12090304 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | isopropyl N-(3-phenylbenzyl)carbamate | HCID 12090303 | 80.6% |
Reaction Steps
1.20 g of isopropyl N-(3-bromobenzyl)carbamate, 0.47 g of sodium carbonate in aqueous solution (20 ml) and 0.10 g of tetrakis(triphenylphosphine)palladium (0) were added to toluene (40 ml) under a nitrogen atmosphere. The resulting solution was mixed with 0.54 g of phenylboric 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 0.85 g of isopropyl N-(3-phenylbenzyl)carbamate as white crystals. m.p. 61-64° C.
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-eddd0fd4e55141ddb28bd22f323e9615 |
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| Source note | uspto-grants-2003_09 |
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