Aluminium lithium hydride → HCID 22763199, compound
Reaction equation
[NH:1]1[CH:5]2[CH:6](Cl)[C:7]3[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=3[C:2]1([O:18][CH2:19][CH2:20][N:21]([CH3:23])[CH3:22])[C:3]1[CH:17]=[CH:16][CH:15]=[CH:14][C:4]=12.[H-].[Al+3].[Li+].[H-].[H-].[H-]>O1CCCC1>[NH:1]1[CH:5]2[CH2:6][C:7]3[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=3[C:2]1([O:18][CH2:19][CH2:20][N:21]([CH3:23])[CH3:22])[C:3]1[CH:17]=[CH:16][CH:15]=[CH:14][C:4]=12Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The compound of Example 8 was dissolved in tetrahydrofuran and added to a suspension of lithium aluminum hydride in tetrahydrofuran and refluxed for 3 hrs. After washing with water, and extraction with ether, the subject compound was obtained; nmr (CDCl3): τ 2.25-3.15 (m, 8H, arom), 5.21 (br d, 1H, J = 5Hz, ##STR17## 5.90-6.90 (m, 5H, PhCH2 --, --OCH2 --, and --NH--), 7.25 (br t, 2H, --CH2N(CH3)2), and 7.63 (s, 6H, --N(CH3)2).
Workup
- temperaturerefluxed for 3 hrs
- washAfter washing with water, and extraction with ether
- customthe subject compound was obtained
Sources & evidence
- ORD record
- ord-2b5d9818a78e4b96b684790439809944
- Source dataset
- uspto-grants-1978_10
- Patent number
- US04123546
Reaction notes
Loading…