2,3-Difluorobenzaldehyde → HCID 66776591, compound

HRID 1169965Notes

Reaction equation

HRID 1169965 reaction equation
C(OC(OCC)[N:5]1[CH:9]=[CH:8][N:7]=[CH:6]1)C.C([Li])CCC.[F:18][C:19]1[C:26]([F:27])=[CH:25][CH:24]=[CH:23][C:20]=1[CH:21]=[O:22]>O1CCCC1>[F:18][C:19]1[C:26]([F:27])=[CH:25][CH:24]=[CH:23][C:20]=1[CH:21]([C:6]1[NH:5][CH:9]=[CH:8][N:7]=1)[OH:22]

Participants

5

Procedure

To a solution of 1-(diethoxymethyl)-1H-imidazole (1.65 ml, 10.1 mmol) in tetrahydrofuran (15 ml), at −60° C. and under nitrogen, was added n-butyllithium (2.5 M in hexanes, 4.03 ml, 10.1 mmol). The reaction mixture was stirred at −60° C. for 1 h, before addition of 2,3-difluorobenzaldehyde (1.00 ml, 9.2 mmol), and then allowed to warm to room temperature over 18 h. The mixture was concentrated in vacuo and to the residue was added ethyl acetate (50 ml) and hydrochloric acid (3M, 50 ml). The two layers were separated and the aqueous phase was basified with aqueous sodium hydroxide solution (20%) and extracted with ethyl acetate (3×100 ml). The combined organic phases were dried (MgSO4) and concentrated in vacuo and the residue was re-crystallised from 2-propanol to give the title compound (1.25 g)

Workup

  1. concentrationThe mixture was concentrated in vacuo and to the residue
  2. additionwas added ethyl acetate (50 ml) and hydrochloric acid (3M, 50 ml)
  3. customThe two layers were separated
  4. extractionextracted with ethyl acetate (3×100 ml)
  5. dry with materialThe combined organic phases were dried (MgSO4)
  6. concentrationconcentrated in vacuo
  7. customthe residue was re-crystallised from 2-propanol

Sources & evidence

ORD record
ord-ba9b3117e56349ed82981baf22799b49
Source dataset
uspto-grants-2010_11
Patent number
US07825149B2

Reaction notes

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