HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxylamine → HCID 18316227, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | 1-Bromo-2-methylpropane | HCID 6555 | — |
| Reactant | 2-Aminobicyclo(2,2,1)heptane-2-carboxylic acid | HCID 115288 | — |
| Reactant | HCID 18315959 | HCID 18315959 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18316227 | HCID 18316227 | — |
Reaction Steps
2-Aminonorbornane-2-carboxylic acid was converted into 2-amino-2-(hydroxymethyl)norbornane as a diastereomeric mixture in a manner analogous to Method B1a. A solution of the amino alcohol (0.31 g, 2.16 mmol) and isobutyl bromide (0.23 ml, 2.16 ml) in DMF (3 mL) was heated at 90° C. for 92 h, then cooled to room temp. and partitioned between EtOAc (100 mL) and a saturated NaHCO3 solution (100 mL). The organic layer was washed with a saturated NaCl solution (50 mL), dried (MgSO4), and concentrated under reduced pressure to yield 2-(isobutylamino)-2-(hydroxymethyl)norbornane as a diastereomeric mixture (0.24 g, 55%): GC-MS m/z 197 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06353006B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-5665a6c847e74a678f1d1fd2c8413c97 |
| Source note | uspto-grants-2002_03 |