Acetic Acid → HCID 22499233, compound

HRID 577638Notes

Reaction equation

HRID 577638 reaction equation
C(N(CC)CC)C.[CH2:8]1[C:12]2=[CH:13][C:14]3[CH2:15][CH2:16][CH2:17][CH2:18][C:19]=3[CH:20]=[C:11]2[CH2:10][CH:9]1[NH2:21].[CH:22](=O)[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C(O)(=O)C>ClCCCl.ClCCl>[CH2:22]([NH:21][CH:9]1[CH2:10][C:11]2=[CH:20][C:19]3[CH2:18][CH2:17][CH2:16][CH2:15][C:14]=3[CH:13]=[C:12]2[CH2:8]1)[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1

Participants

8

Reactant 5

HCID 176Acetic AcidHCID 240BenzaldehydeHCID 8471TriethylamineHCID 5049666Sodium triacetoxyborohydrideHCID 224991882,3,5,6,7,8-Hexahydro-1H-benz[f]inden-2-amine

Product 1

HCID 22499233HCID 22499233, compound

Reagents, catalysts & solvents 2

HCID 111,2-DichloroethaneSolventHCID 6344DichloromethaneSolvent

Procedure

According to the procedure of A. F. Abdel-Magid, et. al. J. Org. Chem. 1996, 61, 3849-3862, triethylamine (0.87 mL, 6.17 mmol) is added to a stirred suspension 2,3,5,6,7,8-hexahydro-1H-cyclopenta[b]naphthalen-2-ylamine in 1,2-dichloroethane (30 mL) under nitrogen at room temperature. Benzaldehyde (0.52 mL, 5.14 mmol) is then added followed by sodium triacetoxyborohydride (1.64 g, 7.7 mmol) and acetic acid (0.44 mL, 7.7 mmol). The reaction is stirred at room temperature for 18 hours. After diluting with dichloromethane the mixture is washed with aqueous NaOH (50 mL, 1M) followed by brine. Removal of the solvent and chromatography (silica, ethyl acetate/hexane, 2:1) affords an oil.

Workup

  1. washis washed with aqueous NaOH (50 mL, 1M)
  2. customRemoval of the solvent and chromatography (silica, ethyl acetate/hexane, 2:1)
  3. customaffords an oil

Sources & evidence

ORD record
ord-952ef91baf6142b3bbb96a2be42e3e3b
Source dataset
uspto-grants-2015_05
Patent number
US09040559B2

Reaction notes

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