HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109289Generated: October 26, 2026
Dimethylformamide → Phenyl N,N-dimethylcarbamate
https://huagongshe.com/reaction/1109289
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-(3,5-Di-tert-butyl-4-hydroxybenzylidene)-2-pyrrolidone | HCID 53896297 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Phenyl N,N-dimethylcarbamate | HCID 138885 | 51% |
Reaction Steps
To a solution of 301 mg of 3-(3,5-di-tert-butyl-4-hydroxybenzylidene)pyrrolidin-2-one (1.0 mmole) dissolved into 5 ml of DMF, NaH (60% in mineral oil, 85 mg, 2.1 mmole) was added under ice-cooling. The resulting mixture was stirred at room temperature for 30 min, then the solution was cooled again. N,N-Dimethylphenylcarbamate (282 mg, 1.71 mmole) which was prepared according to the method described in J. Org. Chem., p660, 21, 1956, was added thereto, then the resulting solution was stirred at room temperature for 3 hours. The reaction mixture was poured into ethyl acetate, which was washed with 1N-HCl, water, and saturated brine, dried over magnesium sulfate, and evaporated. The obtained residue was separated by using silica gel chromatography (toluene:ethyl acetate=2:1) and recrystallized from ether-n-hexane, whereby 190 mg of the objective compound was obtained in 51% yield. The physical constants are described on Table 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05319100 |
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| Source dataset | uspto-grants-1994_06 |
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| ORD ID | ord-280e356f95ab4aec831fb5c6720cbf4a |
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| Source note | uspto-grants-1994_06 |
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