HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → HCID 86664210, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | 3-Hydroxy-4-nitrobenzaldehyde | HCID 69712 | — |
| Reactant | Acetic acid, 2-bromo-2-fluoro-, ethyl ester | HCID 2733407 | — |
| Product | HCID 86664210 | HCID 86664210 | — |
Reaction Steps
Using 3-hydroxy-4-nitrobenzaldehyde as the phenol and ethyl 2-bromo-2-fluoroacetate as the alkylating agent in the general procedure for alkylation of substituted-2-nitrophenols gives a yellow oil: 1H NMR (400 MHz, DMSO-d6) δ ppm 1.26 (t, J=7.07 Hz, 3H), 4.26-4.38 (m, 2H), 6.83 (d, J=55.8 Hz, 1H), 7.76 (dd, J=8.84, 1.26 Hz, 1H), 8.28 (dd, J=8.59, 2.02 Hz, 1H) 8.54 (d, J=2.02 Hz, 1H), 10.02 (s, 1H). ESI-MS: m/z 272.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08669249B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-1b6c84ec0c864df58bfe067f95ee17e1 |
| Source note | uspto-grants-2014_03 |