HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918981Generated: November 1, 2026
Triethylamine → 4-Nitrophenyl ethyl(methyl)carbamate
https://huagongshe.com/reaction/918981
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-Methylethylamine | HCID 12219 | — |
| Reactant | 4-Nitrophenyl chloroformate | HCID 82129 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Nitrophenyl ethyl(methyl)carbamate | HCID 46781556 | 76% |
Reaction Steps
Triethylamine (12.84 g, 127.11 mmol) and p-nitrophenyl chloroformate (63.56 mmol, 12.8 g) were added to a room temperature solution of N-ethylmethylamine (2.50 g, 42.37 mmol) in dry DMF (70 mL) under an argon atmosphere. After 2 h, the reaction mixture was quenched with water, diluted with EtOAc (200 mL), washed with water (2×100 mL), and brine (75 mL). All volatiles were removed under reduced pressure and the residue was purified by SiO2 column chromatography using 10% EtOAc/hexanes to afford compound 4-nitrophenyl ethyl(methyl)carbamate (5.8 g, 76%) as a yellow oil. TLC: 20% EtOAc/hexanes, Rf≈0.50; 1H NMR (CDCl3, 300 MHz) δ 8.18-8.21 (m, 2H), 7.25-7.29 (m, 2H), 3.37-3.46 (m, 2H), 3.05 and 2.97 (s, 3H for two rotamers in 60/40 ratio), 1.17-1.22 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09272991B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-78deda074e8c4650b4074051e1e237be |
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| Source note | uspto-grants-2016_03 |
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