Acetic Acid → HCID 58841404, compound
Reaction equation
[C:1]([O:5][C:6](=[O:21])[N:7]([CH:9]1[C:18]2[C:13](=[CH:14][C:15]([C:19]#N)=[CH:16][CH:17]=2)[O:12][CH2:11][CH2:10]1)[CH3:8])([CH3:4])([CH3:3])[CH3:2].[H-].C([Al+]CC(C)C)C(C)C.CC(O)=[O:34].C(C(C(C([O-])=O)O)O)([O-])=O.[K+].[Na+]>C1(C)C=CC=CC=1.O>[C:1]([O:5][C:6](=[O:21])[N:7]([CH:9]1[C:18]2[C:13](=[CH:14][C:15]([CH:19]=[O:34])=[CH:16][CH:17]=2)[O:12][CH2:11][CH2:10]1)[CH3:8])([CH3:4])([CH3:3])[CH3:2]Participants
Conditions
- Temperature
- -20 °C
Procedure
To a solution of (7-cyano-chroman-4-yl)-methyl-carbamic acid tert-butyl ester (299 mg, 1.04 mmol, 1.0 eq) in anhydrous toluene (5 mL) under N2 at −20° C. was added diisobutylaluminum hydride (Aldrich, 1.50 M in toluene, 1.38 mL, 2.08 mmol, 2.0 eq) slowly. The reaction was stirred at −20° C. for 1 h. Glacial HOAc (1 mL) and H2O (5 mL) was added sequentially. The reaction was warmed to RT spontaneously and stirred at this temperature for an additional 1.5 h. A solution of saturated sodium potassium tartrate (50 mL) was added and the mixture was extracted with EtOAc (60 mL). The aqueous layer was adjusted to pH-10 with 2N NaOH, and extracted with EtOAc (60 mL×2). Combined organic phase was washed with saturated NaCl, dried over Na2SO4, filtered and concentrated. Flash column chromatography (silica gel, 0-8% EtOAc-Hexane) afforded the title compound as a colorless sticky solid.
Workup
- temperatureThe reaction was warmed to RT spontaneously
- stirringstirred at this temperature for an additional 1.5 h
- extractionthe mixture was extracted with EtOAc (60 mL)
- extractionextracted with EtOAc (60 mL×2)
- washCombined organic phase was washed with saturated NaCl
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-69f33d47870f4fb79a2efd29a096b9e1
- Source dataset
- uspto-grants-2008_09
- Patent number
- US07425631B2
Reaction notes
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