Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Methoxy-4-nitroaniline | HCID 7337 | — |
| Reactant | 9-Fluorenylmethyl chloroformate | HCID 34367 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67312186 | HCID 67312186 | 88% |
Reaction Steps
2-methoxy-4-nitroaniline (3 g, 17.8 mmol) was dissolved in THF (60 ml) and pyridine (1.6 ml, 19.6 mmol) was added. The reaction mixture was cooled to 0° C. and Fmoc-Cl (5.07 g, 19.6 mmol) was added in small portions. The reaction was allowed to come to ambient temperature and held for 5 hours. The reaction mixture was concentrated under reduced pressure. The crude product was purified by recrystallisation from CH2Cl2 and MeOH to afford the title compound (6.08 g, 88%). Data: (m/z)=391 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09174940B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-3e3f9769f25143ecb26cbb9015d9b8e7 |
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| Source note | uspto-grants-2015_11 |
|---|