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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1,1-Dibromoethane → Methyl 8-methyl-2,3-dihydro-1,4-benzodioxin-6-carboxylate

HRID 642835
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HRID 642835 반응식
[OH:1][C:2]1[CH:3]=[C:4]([CH:9]=[C:10]([CH3:13])[C:11]=1[OH:12])[C:5]([O:7][CH3:8])=[O:6].C([O-])([O-])=O.[K+].[K+].Br[CH:21](Br)[CH3:22]>C(#N)C>[CH3:13][C:10]1[C:11]2[O:12][CH2:21][CH2:22][O:1][C:2]=2[CH:3]=[C:4]([C:5]([O:7][CH3:8])=[O:6])[CH:9]=1
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참가 물질

5

반응물 3

HCID 112011,1-DibromoethaneHCID 11430Potassium CarbonateHCID 68609716Methyl 3,4-dihydroxy-5-methylbenzoate

생성물 1

HCID 45122025Methyl 8-methyl-2,3-dihydro-1,4-benzodioxin-6-carboxylate

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

A mixture of 34.0 g (0.19 mol) methyl 3,4-dihydroxy-5-methyl-benzoate, 77.12 g (0.56 mol) K2CO3 and 32.1 mL (0.37 mol) dibromoethane in 500 mL acetonitrile was refluxed for 6 h. The solid was filtered off, washed with 100 mL acetonitrile and the filtrate was evaporated to dryness i.vac. The residue was combined with 500 mL water and 500 mL EtOAc, the phases were separated, the organic phase was dried and evaporated to dryness i. vac. The residue was combined with 120 mL DIPE, the precipitate was suction filtered, washed with 50 mL DIPE and dried.

후처리

  1. temperaturewas refluxed for 6 h
  2. filtrationThe solid was filtered off
  3. washwashed with 100 mL acetonitrile
  4. customthe filtrate was evaporated to dryness i.vac
  5. customthe phases were separated
  6. customthe organic phase was dried
  7. customevaporated to dryness i
  8. filtrationfiltered
  9. washwashed with 50 mL DIPE
  10. customdried

출처 및 근거

ORD 기록
ord-a89cb0e2877f49738337f624419e08f9
출처 데이터셋
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07696195B2

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