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Dimethyl Sulfate → 2,3-Dimethoxy-6-nitrobenzaldehyde

HRID 652593
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HRID 652593 반응식
[K].[OH:2][C:3]1[C:10]([O:11][CH3:12])=[CH:9][CH:8]=[C:7]([N+:13]([O-:15])=[O:14])[C:4]=1[CH:5]=[O:6].[C:16](=O)([O-])[O-].[K+].[K+].S(OC)(OC)(=O)=O>CN(C=O)C>[CH3:16][O:2][C:3]1[C:10]([O:11][CH3:12])=[CH:9][CH:8]=[C:7]([N+:13]([O-:15])=[O:14])[C:4]=1[CH:5]=[O:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6497Dimethyl SulfateHCID 11430Potassium CarbonateHCID 867411922-Hydroxy-3-methoxy-6-nitrobenzaldehyde potassium salt

생성물 1

HCID 71721272,3-Dimethoxy-6-nitrobenzaldehyde

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

Potassium salt from Procedure 5 (396 g) was slurried with DMF (8 l) and added to a 1 l flask containing 800 g potassium carbonate. Dimethyl sulfate (420 ml) was added in portions at 60° over 1 hour and the reaction was stirred at 60° overnight. The K2CO3 was washed with acetone and the washings were added to the distillation residue and again solvent was removed in vacuo. The dry residue was treated with water (1 l) and extracted with CH2Cl2. The extracts were dried, evaporated, and the product was crystallized from methanol to afford the product, (335 g, 94%) mp 109°-111° C.

후처리

  1. additionadded to a 1 l flask
  2. washThe K2CO3 was washed with acetone
  3. additionthe washings were added to the distillation residue and again solvent
  4. customwas removed in vacuo
  5. additionThe dry residue was treated with water (1 l)
  6. extractionextracted with CH2Cl2
  7. customThe extracts were dried
  8. customevaporated
  9. customthe product was crystallized from methanol
  10. customto afford the product, (335 g, 94%) mp 109°-111° C.

출처 및 근거

ORD 기록
ord-9c3f3f838afb471c9830b74c270466ec
출처 데이터셋
uspto-grants-1987_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04672116

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