HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344024Generated: October 31, 2026
Allyl bromide → N-t-Butoxycarbonyl-N-allyl-2,2-bis-phenyl-ethylamine
https://huagongshe.com/reaction/344024
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 18787247 | HCID 18787247 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | N-t-Butoxycarbonyl-N-allyl-2,2-bis-phenyl-ethylamine | HCID 54079479 | — |
Reaction Steps
Combine N-t-butoxycarbonyl-2,2-bis-phenyl-ethylamine (2.0 g, 7.73 mmol) and tetrahydrofuran (20 mL) and cool in a dry-ice/acetone bath to -78° C. Slowly, add n-butyllithium (4.4 mL, 1.6M in hexane, 7.04 mmol) and allow to stand for 30 minutes. Add allyl bromide (0.7 mL, 8.09 mmol) maintaining the temperature at -78° C. Warm to ambient temperature and allow to stand for 1.5 hour and then heat to reflux for 5 hours. Cool to ambient temperature and allow to stand for 18 hours. Extract the reaction mixture with a saturated ammonium chloride solution and separate the layers. Extract the aqueous layer with diethyl ether and combine the organic layers. Extract the combine organic layer with water and saturated sodium chloride solution. Separate the organic layer and dry over MgSO4, filter and evaporate in vacuo to obtain a residue. Chromatograph the residue on silica gel eluting with 5% ethyl acetate/hexane to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05864045 |
|---|
| Source dataset | uspto-grants-1999_01 |
|---|
| ORD ID | ord-de1d99e0feee4f97b23426b8a108f27c |
|---|
| Source note | uspto-grants-1999_01 |
|---|