HCID 118151980, compound → HCID 118151864, compound
Reaction equation
C([O:7][CH2:8][CH2:9][C@H:10]1[C@H:14]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[O:13][C:12]2([CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]2)[O:11]1)(=O)C(C)(C)C.C(OCC[C@H]1[C@H](C2C=CC=CC=2)OC2(CCCC2)O1)(=O)C(C)(C)C>>[C:15]1([C@@H:14]2[O:13][C:12]3([CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]3)[O:11][C@H:10]2[CH2:9][CH2:8][OH:7])[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1Participants
3
Procedure
The substantially same method as described in Example 299 was conducted, except that 2-((2S,3S)-3-phenyl-1,4-dioxaspiro[4.5]decan-2-yl)ethyl pivalate (Preparation example 300) was used instead of that 2-((2S,3S)-3-phenyl-1,4-dioxaspiro[4.4]nonan-2-yl)ethyl pivalate (Preparation example 298), to obtain the title compound (1.2 g, 80˜95%)
Sources & evidence
- ORD record
- ord-3ee629dd91234418a98fa5dd3a445472
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09221783B2
Reaction notes
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