Bromine → 6-Bromo-5-methyl-2,3-dihydro-1,4-benzodioxine

HRID 260717노트

반응식

HRID 260717 반응식
[CH3:1][C:2]1[C:11]2[O:10][CH2:9][CH2:8][O:7][C:6]=2[CH:5]=[CH:4][CH:3]=1.[Br:12]Br.S([O-])(O)=O.[Na+]>C(O)(=O)C>[Br:12][C:3]1[CH:4]=[CH:5][C:6]2[O:7][CH2:8][CH2:9][O:10][C:11]=2[C:2]=1[CH3:1]

참가 물질

5

반응물 3

HCID 24408BromineHCID 122388275-Methyl-1,4-benzodioxaneHCID 23665763Sodium Bisulfite

생성물 1

HCID 124645276-Bromo-5-methyl-2,3-dihydro-1,4-benzodioxine수율 98.3%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

In 30 ml of acetic acid, was dissolved 10 g of 5-methyl-1,4-benzodioxane and 11.8 g of bromine was added dropwise to the solution. After stirring for 30 minutes, the reaction mixture was poured into a sodium hydrogen sulfite aqueous solution and extracted with diethyl ether. The resulting diethyl ether layer was washed successively with a sodium hydrogen carbonate aqueous solution, water and saturated saline solution, dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to obtain 15.0 g of 6-bromo-5-methyl-1,4-benzodioxane (bp. 126°-135° C. (7 mmHg)).

후처리

  1. additionwas added dropwise to the solution
  2. extractionextracted with diethyl ether
  3. washThe resulting diethyl ether layer was washed successively with a sodium hydrogen carbonate aqueous solution, water and saturated saline solution
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customthe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-c91ea0b33ad3429f8134c8f646377cb3
출처 데이터셋
uspto-grants-1996_06
특허 번호
US05530021

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