4-Nitrobenzaldehyde → HCID 6610568, compound

HRID 1356435Notes

Reaction equation

HRID 1356435 reaction equation
Cl.[NH2:2][C@H:3]([C:6]([OH:8])=[O:7])[CH2:4][SH:5].C([O-])(=O)C.[Na+].[N+:14]([C:17]1[CH:24]=[CH:23][C:20]([CH:21]=O)=[CH:19][CH:18]=1)([O-:16])=[O:15]>O.C(O)C>[N+:14]([C:17]1[CH:24]=[CH:23][C:20]([CH:21]2[NH:2][C@H:3]([C:6]([OH:8])=[O:7])[CH2:4][S:5]2)=[CH:19][CH:18]=1)([O-:16])=[O:15]

Participants

6

Reactant 3

HCID 5414-NitrobenzaldehydeHCID 60960Cysteine HydrochlorideHCID 517045Sodium Acetate

Product 1

HCID 6610568HCID 6610568, compoundYield 87%

Reagents, catalysts & solvents 2

HCID 702EthanolSolventHCID 962WaterSolvent

Conditions

Temperature
0 °C

Procedure

3 g (17.08 mmoles) of L-Cysteine hydrochloride and 2.18 g (22.2 mmoles) of sodium acetate are dissolved in 75 ml of water. The solution is agitated vigorously during the addition. by portions, of 3.10 g (20.5 mmoles) of 4-nitrobenzaldehyde in solution in 80 ml of 95% ethanol. A white precipitate rapidly appears in this pale yellow solution which forms abundantly. Agitation is maintained for one hour, the reaction mixture is then cooled down to 0° C. and filtered. The precipitate is successively rinsed with 200 ml of water, 100 ml of cold ethanol and 100 ml of ethyl ether. After drying, a white powder is obtained with a yield of 87%. Melting point: 120-121° C.

Workup

  1. temperatureAgitation is maintained for one hour
  2. filtrationfiltered
  3. washThe precipitate is successively rinsed with 200 ml of water, 100 ml of cold ethanol and 100 ml of ethyl ether
  4. customAfter drying
  5. customa white powder is obtained with a yield of 87%

Sources & evidence

ORD record
ord-e5ee257f7ad04865bd0fdf7a4523354c
Source dataset
uspto-grants-2003_07
Patent number
US06586454B2

Reaction notes

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