Tetrabutylammonium Fluoride → HCID 54097675, compound
Reaction equation
[Si]([O:8][C@H:9]1[CH2:18][C@H:17]([O:19][C:20](=[O:33])[C:21]([O:26][C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)([CH3:25])[CH2:22][CH2:23][CH3:24])[C@H:16]2[C:11]([CH:12]=[CH:13][C@H:14]([CH3:51])[C@@H:15]2[CH2:34][CH2:35][C@H:36]2[O:41][C:40](=[O:42])[CH2:39][C@H:38]([O:43][Si](C(C)(C)C)(C)C)[CH2:37]2)=[CH:10]1)(C(C)(C)C)(C)C.[F-].C([N+](CCCC)(CCCC)CCCC)CCC>O1CCCC1>[OH:8][C@H:9]1[CH2:18][C@H:17]([O:19][C:20](=[O:33])[C:21]([O:26][C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)([CH3:25])[CH2:22][CH2:23][CH3:24])[C@H:16]2[C:11]([CH:12]=[CH:13][C@H:14]([CH3:51])[C@@H:15]2[CH2:34][CH2:35][C@H:36]2[O:41][C:40](=[O:42])[CH2:39][C@H:38]([OH:43])[CH2:37]2)=[CH:10]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A procedure similar to that described in Example 2, above, was followed, but using 0.32 g of (4R,6R)-6-([1S,2S,6S,8S,8aR]-2-{1,2,6,7,8,8a-hexahydro-6-t-butyldimethylsilyloxy-8-[(2RS)-2-phenoxy-2-methylvaleryloxy]-2-methyl-1-naphthyl}ethyl)tetrahydro-4-t-butyldimethylsilyloxy-2H-pyran-2-one [prepared as described in Example 88, above] and 6.48 ml of a 1.0 molar solution of tetrabutylammonium fluoride in tetrahydrofuran, to give 0.11 g of the title compound as white crystals, melting at between 151° and 153° C.
Sources & evidence
- ORD record
- ord-023b436c7b1a4d93b06d3bee32a7c716
- Source dataset
- uspto-grants-1996_02
- Patent number
- US05491167
Reaction notes
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