HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373219Generated: October 26, 2026
Dimethylformamide → Tert-butyl[3-(5-benzyloxy-2-nitrophenoxy)benzyl]carbamate
https://huagongshe.com/reaction/1373219
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-butyl N-((3-hydroxyphenyl)methyl)carbamate | HCID 18369568 | — |
| Reactant | 4-Benzyloxy-2-fluoro-1-nitrobenzene | HCID 22180704 | — |
| Solvent | Water | HCID 962 | — |
| Product | Tert-butyl[3-(5-benzyloxy-2-nitrophenoxy)benzyl]carbamate | HCID 21073109 | 95.6% |
Reaction Steps
A mixture of 4-benzyloxy-2-fluoronitrobenzene (6.43 g, 26 mmols), N-tert-butoxycarbonyl-3-hydroxybenzylamine (5.78 g, 26 mmols), potassium carbonate (3.59 g, 26 mmols) and N,N-dimethylformamide (70 ml) was stirred at 100° C. for 12 hours. The reaction mixture was cooled, then poured into water, and extracted with ethyl acetate. The extract was washed with water, and then dried with anhydrous magnesium sulfate, and the solvent was evaporated away to give an yellow oil of tert-butyl[3-(5-benzyloxy-2-nitrophenoxy)benzyl]carbamate (11.2 g, 95.0%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07160887B1 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-7c980fa2674f468087cf3b0e4b38d7d5 |
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| Source note | uspto-grants-2007_01 |
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