Benzaldehyde → HCID 178472685, compound

HRID 402964Notes

Reaction equation

HRID 402964 reaction equation
Cl.[CH2:2]([O:4][C:5](=[O:8])[CH2:6][NH2:7])[CH3:3].[CH:9](=O)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.C(OC)(OC)OC.C(N(CC)CC)C>O.C1(C)C=CC=CC=1.CN1CCCC1=O>[CH2:2]([O:4][C:5](=[O:8])[CH2:6]/[N:7]=[CH:9]/[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[CH3:3]

Participants

8

Conditions

Temperature
5 °C

Procedure

Glycine ethyl ester hydrochloride (69.1 g, 495 mmol) and toluene (215 g) were mixed, and N-methylpyrrolidone (32.5 g) was poured into the mixture at room temperature. Benzaldehyde (50.0 g, 471 mmol) was added dropwise to the obtained mixture, and then trimethyl orthoformate (52.5 g, 495 mmol) was added dropwise. After completion of the dropwise addition, the temperature of the obtained mixture was adjusted to 7° C. and a mixed solution of triethylamine (52.4 g, 518 mmol) and toluene (26.5 g) was added dropwise over 3 hours. After completion of the dropwise addition, the mixture was stirred at a temperature in a range from 7° C. to room temperature for 6 hours. After completion of the reaction, the reaction mixture was cooled to 5° C. and water (140 mL) was added dropwise thereto. Thereafter, stirring was stopped to perform liquid separation and then the obtained organic layer was washed with 20% brine (95 g). The obtained organic layer was dried over magnesium sulfate and the solvent was distilled off under reduced pressure to obtain a toluene solution (104.5 g) of (E)-N-phenylmethyleneglycine ethyl ester (86.9 g of pure (E)-N-phenylmethyleneglycine ethyl ester). Yield: 96%.

Workup

  1. additionAfter completion of the dropwise addition
  2. customwas adjusted to 7° C.
  3. additionAfter completion of the dropwise addition
  4. customAfter completion of the reaction
  5. stirringThereafter, stirring
  6. customliquid separation
  7. washthe obtained organic layer was washed with 20% brine (95 g)
  8. dry with materialThe obtained organic layer was dried over magnesium sulfate
  9. distillationthe solvent was distilled off under reduced pressure

Sources & evidence

ORD record
ord-7e9f95f9563f42f58480c34bbfb04d76
Source dataset
uspto-grants-2014_06
Patent number
US08742162B2

Reaction notes

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