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Oxalic Acid → HCID 13592053, 화합물

HRID 2350985
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HRID 2350985 반응식
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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 971Oxalic AcidHCID 13592052HCID 13592052, 화합물

생성물 1

HCID 13592053HCID 13592053, 화합물수율 76.6%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-0fc42d380b5b42b3ac820169b0648cb7
출처 데이터셋
uspto-grants-1989_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04871762

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