Sodium Iodide → HCID 69429772, compound
Reaction equation
[I-].[Na+].C1OCCOCCOCCOCCOC1.C[O:19][C@H:20]1[CH2:25][CH2:24][CH2:23][C@H:22]([CH2:26][N:27]2[C:35](=[O:36])[C:34]3[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=3)[C:28]2=[O:37])[CH2:21]1.BrB(Br)Br.ClCCl>ClCCl>[OH:19][C@H:20]1[CH2:25][CH2:24][CH2:23][C@H:22]([CH2:26][N:27]2[C:28](=[O:37])[C:29]3[C:34](=[CH:33][CH:32]=[CH:31][CH:30]=3)[C:35]2=[O:36])[CH2:21]1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
Under a nitrogen atmosphere, a solution of sodium iodide (247 mg, 1.65 mmol) and 15-crown-5 (327 μl, 1.65 mmol) in dichloromethane (2.7 ml) was slowly dropped into a solution of trans-2-[(3-methoxycyclohexyl)methyl]-1H-isoindole-1,3(2H)-dione (100 mg, 0.366 mmol) in dichloromethane (2 ml) at −40° C. After 10 minutes, a 1M-tribromoborane-dichloromethane solution (1.10 ml, 1.10 mmol) was added dropwise thereto. After 1 hour, the mixture thus obtained was slowly heated to be adjusted to 0° C. 2.5 hours after the start of the heating. After standing at room temperature for 14 hours, the reaction solution was poured onto ice and extracted with chloroform. The extract solution was concentrated under reduced pressure and the resulting residue was purified by a silica gel column chromatography (eluent: hexane/ethyl acetate) to obtain trans-2-[(3-hydroxycyclohexyl)methyl]-1H-isoindole-1,3(2H)-dione (63.2 mg, 67%).
Workup
- waitAfter 1 hour
- customthe mixture thus obtained
- temperaturewas slowly heated
- customto be adjusted to 0° C
- custom2.5 hours
- waitAfter standing at room temperature for 14 hours
- additionthe reaction solution was poured onto ice
- extractionextracted with chloroform
- concentrationThe extract solution was concentrated under reduced pressure
- customthe resulting residue was purified by a silica gel column chromatography (eluent: hexane/ethyl acetate)
Sources & evidence
- ORD record
- ord-03dbd5ea557f40f39346ec73536285fb
- Source dataset
- uspto-grants-2007_04
- Patent number
- US07199147B2
Reaction notes
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