Aluminium lithium hydride → 1-Amino-2-phenylthio-2-propanol
Reaction equation
[C:1]1([S:7][CH2:8][CH:9]([OH:14])[CH2:10][N:11]=[N+]=[N-])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>O1CCCC1>[C:1]1([S:7][CH2:8][CH:9]([OH:14])[CH2:10][NH2:11])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A procedure similar to that described in Preparation 13 was repeated, except that 8 g of 3-phenylthio-2-hydroxypropylazide (prepared as described in Preparation 86), 2.9 g of lithium aluminum hydride and 400 ml of anhydrous tetrahydrofuran were used, to give 6.8 g of the title compound, melting at 57° C. to 61° C.
Workup
- customA procedure similar to that described in Preparation 13
Sources & evidence
- ORD record
- ord-079868872b804ada9b447e99b25724fd
- Source dataset
- uspto-grants-1996_11
- Patent number
- US05578620
Reaction notes
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