Pyridine → HCID 86586616, compound
Reaction equation
Cl[C:2]([O:4][CH2:5][C:6]([Cl:9])([Cl:8])[Cl:7])=[O:3].N1C=CC=CC=1.[CH:16]([O:19][CH:20]([O:35][CH:36]([CH3:38])[CH3:37])[C:21]([CH3:34])([CH3:33])[C:22](=[O:32])[C@H:23]([CH3:31])[C@@H:24]([OH:30])[C@@H:25]([CH3:29])[CH2:26][CH:27]=[CH2:28])([CH3:18])[CH3:17].[Na+].[Cl-]>C(Cl)Cl>[CH:36]([O:35][CH:20]([O:19][CH:16]([CH3:18])[CH3:17])[C:21]([CH3:33])([CH3:34])[C:22](=[O:32])[C@H:23]([CH3:31])[C@@H:24]([O:30][C:2]([O:4][CH2:5][C:6]([Cl:9])([Cl:8])[Cl:7])=[O:3])[C@@H:25]([CH3:29])[CH2:26][CH:27]=[CH2:28])([CH3:38])[CH3:37]Participants
6
Procedure
Trichloroethyl chloroformate (2.5 mL) and pyridine (2.95 mL) are added to a solution of (4R,5S,6S)-1,1-diisopropoxy-5-hydroxy-2,2,4,6-tetramethyl-8-nonen-3-one (3.0 g) in 40 mL of CH2Cl2 at 0° C., and the mixture is stirred for 5 hours before pouring into sat. aq. NaCl and extracting with CH2Cl2. The extract is dried over Na2SO4, filtered, and evaporated. The product is purified by chromatography on SiO2 (2% ethyl acetate/hexanes).
Workup
- extractionextracting with CH2Cl2
- dry with materialThe extract is dried over Na2SO4
- filtrationfiltered
- customevaporated
- customThe product is purified by chromatography on SiO2 (2% ethyl acetate/hexanes)
Sources & evidence
- ORD record
- ord-7a21ae43a1ad4781932d9bfe71f10c19
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06589968B2
Reaction notes
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