HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 68106974, compound → HCID 68107212, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 68106974 | HCID 68106974 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68107212 | HCID 68107212 | 115% |
Reaction Steps
Methyl 3-(2-methylallyloxy)-4-nitro-benzoate 4a (4.52 g, 18 mmol) was heated to 190° C. and stirred for 3 hours. The reaction mixture was cooled down to room temperature followed by the addition of 50 mL of dichloromethane. The reaction solution was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain the title compound methyl 3-hydroxy-2-(2-methylallyl)-4-nitro-benzoate 4b (2.60 g, yield: 57.7%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08691822B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-9f97467c67744334aeeda8022bbf2a4e |
| Source note | uspto-grants-2014_04 |