4-Toluenesulfonyl chloride → HCID 53762787, compound
Reaction equation
C(O)[CH:2]([OH:8])[CH2:3][CH2:4][CH2:5]CC.C1(C)C=CC(S(Cl)(=O)=O)=CC=1.[C:21]1([CH3:39])[CH:26]=[CH:25][C:24]([S:27]([O:30][CH2:31][CH:32]([OH:38])[CH2:33][CH2:34][CH2:35][CH2:36][CH3:37])(=[O:29])=[O:28])=[CH:23][CH:22]=1>N1C=CC=CC=1>[C:2]([O:38][CH:32]([CH2:33][CH2:34][CH2:35][CH2:36][CH3:37])[CH2:31][O:30][S:27]([C:24]1[CH:23]=[CH:22][C:21]([CH3:39])=[CH:26][CH:25]=1)(=[O:28])=[O:29])(=[O:8])[CH2:3][CH2:4][CH3:5]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Using 1,2-heptanediol, pyridine and p-toluenesulfonyl chloride, (RS)-1-p-toluenesulfonyloxy-2-heptanol 2c ##STR26## was prepared in the same manner as Example 1 of Production.
Workup
- customwas prepared in the same manner as Example 1 of Production
Sources & evidence
- ORD record
- ord-55ec4bf4983e48f4b435ac52416614c1
- Source dataset
- uspto-grants-1988_05
- Patent number
- US04745066
Reaction notes
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