Benzene → HCID 18766757, compound
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
Reactant 3
Product 1
Reagents, catalysts & solvents 1
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
- additionwas added to a three-necked 250-ml round bottom flask
- customequipped with a stirrer
- additiona thermometer and a pressure equilibrating addition funnel
- customcapped with a drying tube
- temperatureThe flask was cooled in an ice bath
- customThe ice bath was removed
- temperaturethe reaction mixture was heated for 1 hr
- customat 48°-58°
- distillationA fractional distillation of the reaction mixture
- 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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