Benzaldehyde → HCID 68534208, compound

HRID 1808233Notes

Reaction equation

HRID 1808233 reaction equation
[F:1][C:2]([F:7])([F:6])[C:3]([OH:5])=[O:4].[NH2:8][CH:9]1[CH2:14][CH:13]2[CH2:15][CH2:16][CH:10]1[CH2:11][C:12]2=[O:17].[CH:18](=O)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>C(Cl)Cl>[F:1][C:2]([F:7])([F:6])[C:3]([OH:5])=[O:4].[C:19]1([CH:18]2[CH:11]3[C:12](=[O:17])[CH:13]4[CH2:15][CH2:16][CH:10]3[CH:9]([CH2:14]4)[NH:8]2)[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1

Participants

4

Procedure

A three neck 3 L flask, fitted with a well isolated soxhlet (300 mL) filled with molecular sieves (3 Å), was charged with 5-amino-bicyclo[2.2.2]octan-2-one trifluoro-acetic acid salt (Preparation 76, 85.0 g, 336 mmol, 1.0 eq), benzaldehyde (37.5 mL, 369 mmol, 1.1 eq) and DCM (1.25 L). The suspension was heated to reflux. The clear reaction mixture was concentrated to a tan solid. The latter was suspended in a mixture of diethyl ether (600 mL) and EtOH (50 mL). The solids were collected by filtration (P3) and thoroughly washed with ethyl acetate and diethyl ether. The filter cake was dried in vacuo to yield title compound as an off-white solid (104 g, 305 mmol, 91%, 97.3% pure (HPLC)).

Workup

  1. customA three neck 3 L flask, fitted with a well isolated soxhlet (300 mL)
  2. additionfilled with molecular sieves (3 Å)
  3. temperatureThe suspension was heated to reflux
  4. concentrationThe clear reaction mixture was concentrated to a tan solid
  5. additionThe latter was suspended in a mixture of diethyl ether (600 mL) and EtOH (50 mL)
  6. filtrationThe solids were collected by filtration (P3)
  7. washthoroughly washed with ethyl acetate and diethyl ether
  8. customThe filter cake was dried in vacuo

Sources & evidence

ORD record
ord-2d652359fcad4f5b8eafc75052ef4c3c
Source dataset
uspto-grants-2013_01
Patent number
US08357711B2

Reaction notes

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