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Thioglycolic Acid → [{(6-Methyl-1,3-benzodioxol-5-yl)methyl}thio]acetic acid

HRID 1195262
ノート
印刷プレビュー

反応式

HRID 1195262 の反応式
Cl[CH2:2][C:3]1[C:11]([CH3:12])=[CH:10][C:6]2[O:7][CH2:8][O:9][C:5]=2[CH:4]=1.[SH:13][CH2:14][C:15]([OH:17])=[O:16].[OH-].[Na+].C(Cl)(Cl)Cl>C(O)C>[CH3:12][C:11]1[C:3]([CH2:2][S:13][CH2:14][C:15]([OH:17])=[O:16])=[CH:4][C:5]2[O:9][CH2:8][O:7][C:6]=2[CH:10]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 1133Thioglycolic AcidHCID 6212ChloroformHCID 14798Sodium HydroxideHCID 105594165-(Chloromethyl)-6-methylbenzo[d][1,3]dioxole

生成物 1

HCID 14514915[{(6-Methyl-1,3-benzodioxol-5-yl)methyl}thio]acetic acid収率 20.5%

試薬・触媒・溶媒 1

HCID 702Ethanol
溶媒

実験手順

A suspension of 6.0 g of 5-chloromethyl-6-methyl-1,3-benzodioxole, 6.0 g of mercaptoacetic acid and 6.5 g of sodium hydroxide in 130 ml of 50% hydrous ethanol was heated under reflux for 1 h. The reaction mixture was concentrated. Water was added thereto and the mixture was washed with ethyl acetate. The aqueous layer was acidified with 1Nhydrochloric acid. After extraction with chloroform, the extract was dried over magnesium sulfate. The solvent was distilled off and the product was isolated according to silica gel column chromatography (chloroform). The crystals thus obtained were recrystallized from diisopropyl ether to obtain 1.6 g of the intended compound in the form of white crystals.

後処理

  1. temperaturewas heated
  2. temperatureunder reflux for 1 h
  3. concentrationThe reaction mixture was concentrated
  4. additionWater was added
  5. washthe mixture was washed with ethyl acetate
  6. extractionAfter extraction with chloroform
  7. dry with materialthe extract was dried over magnesium sulfate
  8. distillationThe solvent was distilled off
  9. customthe product was isolated
  10. customThe crystals thus obtained
  11. customwere recrystallized from diisopropyl ether

出典と根拠

ORDレコード
ord-a2af1832291d4b2091218f9a6db55ce9
出典データセット
uspto-grants-1992_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05110956

反応ノート

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