HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-bromo-N-(2-methylbut-3-yn-2-yl)benzenamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Bromoaniline | HCID 7807 | — |
| Reactant | 1-Butyne, 3-chloro-3-methyl- | HCID 70679 | — |
| Catalyst | Copper | HCID 23978 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-bromo-N-(2-methylbut-3-yn-2-yl)benzenamine | HCID 20082271 | — |
Reaction Steps
To a solution of 4-bromobenzenamine (4.0 g, 23 mmol), TEA (4.3 ml, 31 mmol), 2.0 ml of water, copper (0.058 g, 0.91 mmol) and copper(I) chloride (0.058 g, 0.59 mmol) in diethyl ether (9.8 ml, 20 mmol) was added 3-chloro-3-methylbut-1-yne (2.0 g, 20 mmol), dropwise. After stirring overnight, the reaction mixture was transferred to a seperatory funnel containing water and diethyl ether. The aqueous layer was washed 3× with EtOAc. The organic layers were combined, dried with MgSO4, filtered and concentrated. The crude oil was purified with by MPLC (100% DCM to 10% (91/10/1 DCM:MeOH:NH4OH)) to provide the product as an oil. MS m/z: 240 (M+2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07973047B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-2df9bcd7cc664ae0af973b6eb19e64f1 |
| Source note | uspto-grants-2011_07 |