Ethyl 6-hydroxyhexanoate → Ethyl 6-((tert-butyldimethylsilyl)oxy)hexanoate
Reaction equation
[OH:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]([O:9][CH2:10][CH3:11])=[O:8].[Si:12](OC(CCC)CC(OCC)=O)([C:15]([CH3:18])([CH3:17])[CH3:16])([CH3:14])[CH3:13]>>[Si:12]([O:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]([O:9][CH2:10][CH3:11])=[O:8])([C:15]([CH3:18])([CH3:17])[CH3:16])([CH3:14])[CH3:13]Participants
3
Procedure
Ethyl 6-((tert-butyldimethylsilyl)oxy)hexanoate 8 (3.08 g) was prepared in 90% yield using ethyl 6-hydroxyhexanoate 7 according to the procedures described for compound 2 in above (see Schemes 1-3).
Sources & evidence
- ORD record
- ord-33b678d928f24c988ed33f52f0f4cbaa
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09315486B2
Reaction notes
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