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3,4-Dichlorobenzoic acid → 3,4-Dichloro-2-methylbenzoic acid

HRID 1492392
ノート
印刷プレビュー

反応式

HRID 1492392 の反応式
[CH2:1]([Li])CCC.[Cl:6][C:7]1[CH:8]=[C:9]([CH:13]=[CH:14][C:15]=1[Cl:16])[C:10]([OH:12])=[O:11].CI>O1CCCC1>[Cl:6][C:7]1[C:8]([CH3:1])=[C:9]([CH:13]=[CH:14][C:15]=1[Cl:16])[C:10]([OH:12])=[O:11]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 58173,4-Dichlorobenzoic acidHCID 6328Methyl iodideHCID 178418339Butyllithium

生成物 1

HCID 105843563,4-Dichloro-2-methylbenzoic acid

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

n-Butyl lithium (2.5M in hexanes, 180 ml) was added during 1 hour to a stirred solution of 3,4-dichlorobenzoic acid (40.0 g) at -78° C. and stirring maintained at that temperature overnight. A solution of methyl iodide (72 ml) in tetrahydrofuran was then added during 1.5 hours and the mixture kept at -78° C. for 3 hours and allowed to warm to room temperature overnight. The solvent was evaporated and the mixture added to water, acidified (concentrated hydrochloric acid) and extracted (ethyl acetate). The extract was dried (magnesium sulphate), evaporated and triturated (ether) to give 3,4-dichloro-2-methylbenzoic acid (33.3 g) as a white solid, m.p. 177°-178° C.

後処理

  1. temperaturemaintained at that temperature overnight
  2. customThe solvent was evaporated
  3. additionthe mixture added to water
  4. extractionextracted (ethyl acetate)
  5. dry with materialThe extract was dried (magnesium sulphate)
  6. customevaporated
  7. customtriturated (ether)

出典と根拠

ORDレコード
ord-dd024062847c4be5855e0e098498a274
出典データセット
uspto-grants-1994_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05374606

反応ノート

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