Benzene → HCID 18766757, compound

HRID 1658616Notes

Reaction equation

HRID 1658616 reaction equation
[CH2:1]([N:3]([CH2:5][CH3:6])[NH2:4])[CH3:2].C1C=CC=CC=1.[C:13](OC(=O)C)(=[O:15])[CH3:14]>C(Cl)(Cl)(Cl)Cl>[CH2:1]([N:3]([CH2:5][CH3:6])[NH:4][C:13](=[O:15])[CH3:14])[CH3:2]

Participants

5

Procedure

N',N'-diethylacethydrazide was prepared following essentially the teaching of Hinman and Fulton, J. Amer. Chem. Soc. 80, 1895-1900 (1958). A mixture of 8.2 g (0.094 mole) of freshly distilled N,N-diethylhydrazine and 75 ml of benzene was added to a three-necked 250-ml round bottom flask equipped with a stirrer, a thermometer and a pressure equilibrating addition funnel capped with a drying tube. The flask was cooled in an ice bath. To this stirred solution was added 12.3 g (0.12 mole) of acetic anhydride. The ice bath was removed and the reaction mixture was heated for 1 hr. at 48°-58°. A fractional distillation of the reaction mixture gave a cut, b.p. 83°-84° at 3 mm, which melted at 47.5°-49.5°. NMR (CCl4, TMS) τ 1.0 (3 H, t), 1.9 (3 H, s), 2.6 (2 H, quad), 8.5 (1 H, broad).

Workup

  1. additionwas added to a three-necked 250-ml round bottom flask
  2. customequipped with a stirrer
  3. additiona thermometer and a pressure equilibrating addition funnel
  4. customcapped with a drying tube
  5. temperatureThe flask was cooled in an ice bath
  6. customThe ice bath was removed
  7. temperaturethe reaction mixture was heated for 1 hr
  8. customat 48°-58°
  9. distillationA fractional distillation of the reaction mixture
  10. customgave a cut, b.p. 83°-84° at 3 mm, which melted at 47.5°-49.5°

Sources & evidence

ORD record
ord-578758ff4e554d42b7ae65defc2c9ed0
Source dataset
uspto-grants-1976_06
Patent number
US03965174

Reaction notes

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