Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Methoxybenzyl alcohol | HCID 7738 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyl [(5-chloro-2-nitrophenyl)methyl]carbamate | HCID 71357443 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86661624 | HCID 86661624 | 99% |
Reaction Steps
Sodium hydride (63%, 25 g, 656 mmol) was added to a solution of 4-methoxybenzyl alcohol (90.3 g, 654 mmol) and tert-butyl (5-chloro-2-nitrophenyl)methylcarbamate (US200216506 A1, 156 g, 544 mmol) in DMF (1.4 L) at room temperature, and the mixture was stirred at 80° C. for four hours. After leaving to cool, water (1.5 L) was added to the reaction mixture. The precipitated solid was collected by filtration to obtain the title compound (209 g, 99%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946264B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-93ffd683b57d413183d662e8d9ca45fe |
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| Source note | uspto-grants-2015_02 |
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