Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | HCID 67373781 | HCID 67373781 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67373930 | HCID 67373930 | — |
Reaction Steps
A solution of the material from Step A above (25 mg) was dissolved in 1 mL of THF and cooled to 0° C. Triethylamine (25 μL) was added, followed by 4 mg of triphosgene. The reaction stirred for 5 minutes at 0° C., then 5 minutes at room temperature and then was recooled to 0° C. and stirred for 5 minutes more. A solution of 4-methoxyaniline in 1 mL of THF was added slowly. The reaction was stirred for 40 minutes, diluted with EtOAc and washed with 10% citric acid solution, saturated NaHCO3 and brine. The solution was dried (Na2SO4) and concentrated in vacuo to give the titled product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08008295B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-329abdfc47e148929dfa89f6f78c96cf |
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| Source note | uspto-grants-2011_08 |
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