Methanesulfonyl chloride → HCID 22009796, compound
Reaction equation
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([CH2:15][CH2:16][CH2:17][CH2:18][OH:19])[CH:12]=[CH:13][CH:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:20][S:21](Cl)(=[O:23])=[O:22]>>[CH3:20][S:21]([O:19][CH2:18][CH2:17][CH2:16][CH2:15][C:11]1[CH:12]=[CH:13][CH:14]=[C:9]([O:8][CH2:1][C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[CH:10]=1)(=[O:23])=[O:22]Participants
3
Procedure
In substantially the same manner as in Reference Example 85, 4-(3-benzyloxyphenyl)butanol was allowed to react with methanesulfonylchloride to give 4-(3-benzyloxyphenyl)butyl methanesulfonate. The yield was quantative. Oily substance.
Sources & evidence
- ORD record
- ord-16451b7123954b68925bbdb01707579f
- Source dataset
- uspto-grants-2001_04
- Patent number
- US06211215B1
Reaction notes
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