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

HRID 1492392
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HRID 1492392 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

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

생성물 1

HCID 105843563,4-Dichloro-2-methylbenzoic acid

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

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.

후처리

  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)

출처 및 근거

ORD 기록
ord-dd024062847c4be5855e0e098498a274
출처 데이터셋
uspto-grants-1994_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05374606

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