HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Bromo-1-hexanol → N-ethyl-N-(6-hydroxyhexyl)-4-bromoaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Bromo-1-hexanol | HCID 77970 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-bromo-N-ethylaniline | HCID 11745656 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-ethyl-N-(6-hydroxyhexyl)-4-bromoaniline | HCID 18793525 | 100% |
Reaction Conditions
| Temperature | 110 °C |
|---|
Reaction Steps
36.8 g (184.1 mmols) of N-ethyl-4-bromoaniline, 48.1 ml (1.5-fold equivalent weight) of N,N-diisopropylethylamine and 28.9 ml (1.2 equivalent) of 6-bromohexanol were mixed, and the mixture obtained was heated at 110° C. for 14 hours in an atmosphere of argon. Water was added to the reaction solution obtained, which was then extracted with ethyl acetate. The organic layer obtained was dried with anhydrous magnesium sulfate and then concentrated. The residue thus obtained was heated under reduced pressure (160° C./0.3 torr), and the components distilled out were removed to obtain 55.6 g of crude N-ethyl-N-(6-hydroxyhexyl)-4-bromoaniline (yield: 100%; a dark-brown oily liquid).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06051722 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-43f38d4b835a4852888afb02c2db9b16 |
| Source note | uspto-grants-2000_04 |