Hexane → HCID 12143937、化合物

HRID 916203

反応式

HRID 916203 の反応式
[Cl:1][C:2]1[CH:8]=[C:7]([CH3:9])[CH:6]=[C:5]([CH3:10])[C:3]=1[NH2:4].C(N(C(C)C)CC)(C)C.[Cl:20][CH2:21][CH2:22][CH2:23][CH2:24][C:25](Cl)=[O:26].CCCCCC>C1COCC1.C(OCC)C>[Cl:1][C:2]1[CH:8]=[C:7]([CH3:9])[CH:6]=[C:5]([CH3:10])[C:3]=1[NH:4][C:25](=[O:26])[CH2:24][CH2:23][CH2:22][CH2:21][Cl:20]

参加物

7

実験手順

To a solution of 2-chloro-4,6-dimethylaniline (14.7 g) and diisopropylethylamine (18 mL) in 150 mL of THF, was added a solution of 5-chlorovaleryl chloride (12.2 mL) in 75 mL of THF. After the reaction mixture had been allowed to stir at room temperature overnight, it was filtered and the filtrate concentrated on the rotary evaporator. The residue was dissolved in ethyl acetate and washed with 1 M aqueous HCl, saturated aqueous sodium bicarbonate, and brine. The ethyl acetate solution was then dried with magnesium sulfate and concentrated on the rotary evaporator to give a solid which was combined with a 1:1 mixture of hexane and diethyl ether. After this mixture had been stirred for an hour, it was filtered and the collected solids were dried to provide 12.2 g of 5-chloropentanoic acid (2-chloro-4,6-dimethylphenyl)amide, mp 80.6-82.9° C.

後処理

  1. filtrationit was filtered
  2. concentrationthe filtrate concentrated on the rotary evaporator
  3. dissolutionThe residue was dissolved in ethyl acetate
  4. washwashed with 1 M aqueous HCl, saturated aqueous sodium bicarbonate, and brine
  5. dry with materialThe ethyl acetate solution was then dried with magnesium sulfate
  6. concentrationconcentrated on the rotary evaporator
  7. customto give a solid which
  8. stirringAfter this mixture had been stirred for an hour
  9. filtrationit was filtered
  10. customthe collected solids were dried

出典と根拠

ORDレコード
ord-dad4dcf086f74905b22abda7b8b6fef1
出典データセット
uspto-grants-2007_09
特許番号
US07268146B2

関連ノート

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