Hydrochloric Acid → HCID 21490901、化合物
反応式
Cl.[K].[C:3]([C:6]1[CH:11]=[C:10]([Cl:12])[C:9]([CH2:13][CH2:14][CH2:15][CH3:16])=[C:8]([Cl:17])[N:7]=1)([OH:5])=[O:4].[CH3:18]O>>[CH3:18][O:4][C:3]([C:6]1[CH:11]=[C:10]([Cl:12])[C:9]([CH2:13][CH2:14][CH2:15][CH3:16])=[C:8]([Cl:17])[N:7]=1)=[O:5]参加物
5
実験手順
300 ml of 5 N hydrochloric acid in methanol are added to 28.6 g (0.1 mol) of the potassium salt of 2-carboxy-4,6-dichloro-5-n-butyl-pyridine and the mixture is heated for 8 hours under reflux. It is then evaporated to dryness and hydrochloric acid which still adheres is distilled off with toluene. The residue is rendered alkaline with 2 N sodium carbonate solution and extracted with ether. The ether phases are combined, dried with sodium sulphate and evaporated. Distillation of the residue in a bulb tube at a temperature of 140°-160° at 0.3 mm Hg yields 2-methoxycarbonyl-4,6-dichloro-5-n-butyl-pyridine of the formula ##STR31##
後処理
- temperaturethe mixture is heated for 8 hours
- temperatureunder reflux
- customIt is then evaporated to dryness and hydrochloric acid which
- distillationstill adheres is distilled off with toluene
- extractionextracted with ether
- dry with materialdried with sodium sulphate
- customevaporated
- distillationDistillation of the residue in a bulb tube at a temperature of 140°-160° at 0.3 mm Hg
出典と根拠
- ORDレコード
- ord-063305cf5cb84c39b55c9ecf63a9dda3
- 出典データセット
- uspto-grants-1976_12
- 特許番号
- US03998955
反応ノート
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