HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-methyl-N-[2-((1S,2S,5S)-6,6-dimethylbicyclo[3,1,1]hept-2-yl)-ethyl]-2-aminoethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-Methylaminoethanol | HCID 5247031 | — |
| Reactant | (1S,2S,5S)-2-(2-bromoethyl)-6,6-dimethylbicyclo[3.1.1]heptane | HCID 22850929 | — |
| Product | N-methyl-N-[2-((1S,2S,5S)-6,6-dimethylbicyclo[3,1,1]hept-2-yl)-ethyl]-2-aminoethanol | HCID 22850950 | — |
Reaction Steps
3.4 ml N-methylaminoethanol and 7.3 ml triethylamine were added to 12.4 g 2-((1S,2S,5S)-6,6-dimethylbicyclo[3,1,1]hept-2-yl)-ethyl bromide, and the reaction mixture was stirred for 6 hours at room temperature. To work up the reaction mixture it was chromatographed over silica gel using dichloromethane/methanol (8:2) as solvent. 3.8 g N-methyl-N-[2-((1S,2S,5S)-6,6-dimethylbicyclo[3,1,1]hept-2-yl)-ethyl]-2-aminoethanol were obtained. Rf value=0.4. Furthermore, 7 g unreacted starting material were recovered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05294638 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-3b917bd3c4394f31aa22d87034678140 |
| Source note | uspto-grants-1994_03 |