HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloro-4-nitrobenzene → 4-nitro-N-(tetrahydrofuran-2-ylmethyl)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloro-4-nitrobenzene | HCID 7474 | — |
| Reactant | Tetrahydrofurfurylamine | HCID 253298 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-nitro-N-(tetrahydrofuran-2-ylmethyl)aniline | HCID 22610593 | — |
Reaction Steps
0.3 mol (46.2 g) of para-chloronitrobenzene and 1 mol (101 g) of tetrahydrofurfurylamine are heated for three hours in an oil bath at 150° C. The reaction medium is then poured into 500 ml of ice-cooled water. The expected product initially precipitates in the form of a thick oil which rapidly crystallises. After it has been filtered off, washed with water, recrystallised from ethanol and dried in vacuo, the product melts at 74° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04149848 |
| Source dataset | uspto-grants-1979_04 |
| ORD ID | ord-8e760d57566e4935a58717f2a533efcf |
| Source note | uspto-grants-1979_04 |