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Chlorosuccinimide → Methyl 7-chloro-2,3-dihydro-8-methoxy-1,4-benzodioxin-5-carboxylate

HRID 1868355
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반응식

HRID 1868355 반응식
[CH3:1][O:2][C:3]1[C:8]2[O:9][CH2:10][CH2:11][O:12][C:7]=2[C:6]([C:13]([O:15][CH3:16])=[O:14])=[CH:5][CH:4]=1.[Cl:17]N1C(=O)CCC1=O>C(#N)C>[Cl:17][C:4]1[CH:5]=[C:6]([C:13]([O:15][CH3:16])=[O:14])[C:7]2[O:12][CH2:11][CH2:10][O:9][C:8]=2[C:3]=1[O:2][CH3:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 31398ChlorosuccinimideHCID 11637164HCID 11637164, 화합물

생성물 1

HCID 11565132Methyl 7-chloro-2,3-dihydro-8-methoxy-1,4-benzodioxin-5-carboxylate

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

A mixture of intermediate (1) (0.118 mol) and N-chlorosuccinimide (0.125 mol) in ACN (350 ml) was stirred at room temperature for two days. The solvent was evaporated and the residue was partitioned between DCM (500 ml) and water (500 ml). The organic layer was separated, dried, filtered and the solvent was evaporated. A part of the residue was crystallized from a mixture of DIPE and ACN, yielding methyl 7-chloro-2,3-dihydro-8-methoxy-1,4-benzodioxin-5-carboxylate (intermediate 2, mp. 99° C.)

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후처리

  1. customThe solvent was evaporated
  2. customthe residue was partitioned between DCM (500 ml) and water (500 ml)
  3. customThe organic layer was separated
  4. customdried
  5. filtrationfiltered
  6. customthe solvent was evaporated
  7. customA part of the residue was crystallized from a mixture of DIPE and ACN

출처 및 근거

ORD 기록
ord-ac8a1a8dcfe64a0db7b999b733f439bf
출처 데이터셋
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07635706B2

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