2-Phenylethanol → HCID 58648560, compound
Reaction equation
[O:1]=[C:2]([N:10]1[CH2:14][CH2:13][CH2:12][C@H:11]1[C:15]([OH:17])=[O:16])[C:3](=[O:9])[C:4]([CH3:8])([CH3:7])[CH2:5][CH3:6].[CH2:18](O)[CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1.C1(N=C=NC2CCCCC2)CCCCC1.C12(CS(O)(=O)=O)C(C)(C)C(CC1)CC2=O>CN(C)C1C=CN=CC=1.C(Cl)Cl>[CH3:8][C:4]([CH3:7])([CH2:5][CH3:6])[C:3](=[O:9])[C:2]([N:10]1[CH2:14][CH2:13][CH2:12][C@H:11]1[C:15]([O:17][CH2:18][CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)=[O:16])=[O:1]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of (2S)-1-(1,2-dioxo-3,3-dimethylpentyl)-2-pyrrolidine-carboxylic acid (570 mg; 2.36 mmol), phenethyl alcohol (432 mg; 3.54 mmol), dicyclohexylcarbodiimide (780 mg; 3.78 mmol), 4-dimethylaminopyridine (98 mg; 0.79 mmol) and camphorsulphonic acid (183 mg; 0.79 mmol) in methylene chloride (30 mL) was stirred overnight under a nitrogen atmosphere. The reaction mixture was filtered through Celite to remove solids and concentrated in vacuo, and the crude material was purified on a flash column (25% ethyl acetate in hexane) to obtain 600 mg of the product as a colorless oil. 1H NMR (CDCl3; 300 MHz) δ0.87 (t, 3H); 1.21 (s, 3H); 1.25 (s, 3H); 1.64–1.94 (m, 6H); 2.17 (m, 1H); 2.97 (m, 2H); 3.49 (m, 2H); 4.36 (m, 2H); 4.51 (m, 1H); 7.22–7.33 (m, 5H).
Workup
- filtrationThe reaction mixture was filtered through Celite
- customto remove solids
- concentrationconcentrated in vacuo
- customthe crude material was purified on a flash column (25% ethyl acetate in hexane)
Sources & evidence
- ORD record
- ord-f49ebe3996c149caa91dede07a848e2f
- Source dataset
- uspto-grants-2006_06
- Patent number
- US07056935B2
Reaction notes
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