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Oxalic Acid → HCID 13592053、化合物

HRID 2350985
ノート
印刷プレビュー

反応式

HRID 2350985 の反応式
C(OC([O:6][C:7]1[C:8]([CH3:18])=[C:9]([CH3:17])[C:10]2[O:14][CH2:13][S:12][C:11]=2[C:15]=1[CH3:16])C)C.C(O)(=O)C(O)=O>C(Cl)Cl>[OH:6][C:7]1[C:8]([CH3:18])=[C:9]([CH3:17])[C:10]2[O:14][CH2:13][S:12][C:11]=2[C:15]=1[CH3:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 971Oxalic AcidHCID 13592052HCID 13592052、化合物

生成物 1

HCID 13592053HCID 13592053、化合物収率 76.6%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

5.0 g of 5-(1-ethoxyethoxy)-4,6,7-trimethyl-1,3-benzoxathiole (prepared as described in Example 63) were dissolved in 20 ml of methylene chloride, and 10 g of silica gel-60 (a product of Merck and Co., Inc.) and 1 ml of a 10% w/v aqueous solution of oxalic acid were added. The mixture was then reacted for 1.5 hours at room temperature, after which the silica gel was filtered off. The methylene chloride was then distilled from the solution to yield a crude product, which was extracted with benzene. The extract was dried over anhydrous sodium sulfate, and the benzene was distilled off to yield crude crystals, which were recrystallized from an approximately 10:1 by volume mixture of benzene and petroleum ether, to yield 2.8 g of the title compound, melting at 131°-132° C.

後処理

  1. customThe mixture was then reacted for 1.5 hours at room temperature
  2. filtrationafter which the silica gel was filtered off
  3. distillationThe methylene chloride was then distilled from the solution
  4. customto yield a crude product, which
  5. extractionwas extracted with benzene
  6. dry with materialThe extract was dried over anhydrous sodium sulfate
  7. distillationthe benzene was distilled off
  8. customto yield crude crystals, which
  9. customwere recrystallized from an approximately 10:1 by volume mixture of benzene and petroleum ether

出典と根拠

ORDレコード
ord-0fc42d380b5b42b3ac820169b0648cb7
出典データセット
uspto-grants-1989_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04871762

反応ノート

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