HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexane → HCID 20333854, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | Nitrogen oxide (N2O4) | HCID 25352 | — |
| Reactant | HCID 20333853 | HCID 20333853 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 20333854 | HCID 20333854 | — |
Reaction Steps
A solution of 3-(2-bromo-5-chloro-3-benzofuranyl)phenylacetic acid in chloroform with 1.5 equivalents of cyclohexane is treated with 1.5 equivalents of dinitrogen tetroxide and stirred for about 20 hours at room temperature. The mixture is washed with water, extracted with saturated sodium bicarbonate solution, then the aqueous extracts are acidified. The mixture is extracted with dichloromethane, which is dried and concentrated. The residue is recrystallized from a mixture of benzene and hexane to provide 3-(5-chloro-2-nitro-3-benzofuranyl)phenylacetic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04066782 |
| Source dataset | uspto-grants-1978_01 |
| ORD ID | ord-18f33c65853545ecaffca25f752e6073 |
| Source note | uspto-grants-1978_01 |