HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114177Generated: October 26, 2026
Benzyl Alcohol → 5-benzyloxy-N,N-dimethyl-2-nitrobenzamide
https://huagongshe.com/reaction/2114177
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Chloro-N,N-dimethyl-2-nitrobenzamide | HCID 22934807 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-benzyloxy-N,N-dimethyl-2-nitrobenzamide | HCID 23130267 | 89.8% |
Reaction Steps
Sodium hydride (210 mg) was suspended in DMF (10 mL), and the suspension was cooled to 0° C. and thereto were added benzyl alcohol (568 mg) and a solution of 5-chloro-N,N-dimethyl-2-nitrobenzamide (1.00 g) in DMF (2 mL). The mixture was stirred at 50° C. for 0.5 hour and then concentrated. The residue was acidified with 2N hydrochloric acid and extracted with ethyl acetate. The extract was washed with water and concentrated. The residue was purified by column chromatography on silica gel (ethyl acetate:hexane=1:2→2:3) to give 5-benzyloxy-N,N-dimethyl-2-nitrobenzamide (1.18 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07432392B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-fc65824a0cfa40f8a7587440764e6c86 |
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| Source note | uspto-grants-2008_10 |
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