Acetic Acid → HCID 137252530, compound
Reaction equation
[O:1]([CH2:8][C:9]([NH:11][C@@H:12]1[C:44](=[O:45])[N:14]2[CH:15]([C:38]([O:40]CC=C)=[O:39])[C:16]([CH2:19][O:20][C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=3[C:27]3[NH:36][C:35](=[O:37])[C:34]4[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=4)[N:28]=3)=[CH:17][S:18][C@H:13]12)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(C(CCCC)C([O-])=O)C.[Na+].C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.CC(O)=O>C(Cl)Cl.C(OCC)(=O)C.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[O:1]([CH2:8][C:9]([NH:11][C@@H:12]1[C:44](=[O:45])[N:14]2[CH:15]([C:38]([OH:40])=[O:39])[C:16]([CH2:19][O:20][C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=3[C:27]3[NH:36][C:35](=[O:37])[C:34]4[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=4)[N:28]=3)=[CH:17][S:18][C@H:13]12)=[O:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
8
Reactant 4
Product 1
Reagents, catalysts & solvents 3
Procedure
Compound 9 and 10 (0.071 g, 0.114 mmol) were dissolved in 5 mL of dry methylene chloride. Sodium 2-ethylhexanoate (0.019 g, 0.11 mmol) was dissolved in 2 mL of ethyl acetate. After these two solutions were mixed together, PPh3 (0.01 g, 0.04 mmol) and Pd(PPh3)4 (0.01 g, 0.009 mmol) were added. The combined reaction mixture was stirred for 1.5 h at rt. AcOH (0.5 mL) was added to the solution and the reaction mixture was evaporated in vacuo. The residue was re-evaporated from toluene to yield two separable isomers, 23 and 24 (0.09 g). The crude product was used for the next step without any purification.
Workup
- additionAfter these two solutions were mixed together
- customThe combined reaction mixture
- customthe reaction mixture was evaporated in vacuo
- customThe residue was re-evaporated from toluene
Sources & evidence
- ORD record
- ord-de974a9cfe664d3cac278e90ee32c41e
- Source dataset
- uspto-grants-2012_11
- Patent number
- US08318450B2
Reaction notes
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