HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrophenol → Chloromethyl 4-nitrophenyl carbonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrophenol | HCID 980 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Chloromethyl chloroformate | HCID 62754 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Chloromethyl 4-nitrophenyl carbonate | HCID 2777826 | 95% |
Reaction Steps
p-Nitrophenol (100 g, 0.72 moles) was dissolved in anhydrous tetrahydrofuran (3 L) and stirred vigorously. To this solution was added chloromethyl chloroformate (70 mL, 0.79 moles) at room temperature followed by triethylamine (110 mL). After stirring for 1 hour, the reaction mixture was filtered and the filtrate was concentrated and then diluted with ethyl acetate (1 L). The organic solution was washed with 10% potassium carbonate (3×500 mL) and 1N HCl (2×300 mL), brine (2×300 mL) and dried over anhydrous sodium sulfate. Removal of the solvent gave 157 g (95%) of the title compound (52) as a solid. The compound was unstable to LC-MS. 1H NMR (CDCl3, 400 MHz): 5.86 (s, 2H), 7.44 (d, J=9 Hz, 2H), 8.33 (d, J=9 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06972341B2 |
| Source dataset | uspto-grants-2005_12 |
| ORD ID | ord-e5c4179a8bd54ba386622b5bb3829bad |
| Source note | uspto-grants-2005_12 |