2-Methoxyethanol → HCID 18646613, compound
Reaction equation
Cl[C@H:2]1[C@H:14]2[C@H:10]([N:11]=[C:12]([C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)[O:13]2)[CH2:9][C:8]2[CH:7]=[CH:6][CH:5]=[CH:4][C:3]1=2.[Li].C[O:23]CCO>O>[C:15]1([C:12]2[O:13][C@H:14]3[CH:2]([OH:23])[C:3]4[CH:4]=[CH:5][CH:6]=[CH:7][C:8]=4[CH2:9][C@H:10]3[N:11]=2)[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 90 °C
Procedure
To a solution of (±)-(3aR,9R, 9aR)-9-chloro-3a, 4,9,9a-tetrahydro-2-phenyl-naphth[2,3-d]oxazole (360 mg) in 2-methoxyethanol (10 ml) was added a solution of lithium hydroxyde monohydrate (67 mg) in water (2 ml). The mixture was warmed at 90° C. for 1/2 hour and the title compound was precipitated by addition of water. Filtration, washing with water and drying in vacuo gave the title compound as a yellow solid (205 mg).
Workup
- customthe title compound was precipitated by addition of water
- filtrationFiltration
- washwashing with water
- customdrying in vacuo
Sources & evidence
- ORD record
- ord-3573b11624c343abae81e3e89c64216e
- Source dataset
- uspto-grants-1991_08
- Patent number
- US05041673
Reaction notes
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