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Ethanol → 4-Fluoro-1,2-benzenediol

HRID 2226095
ノート
印刷プレビュー

反応式

HRID 2226095 の反応式
B(Br)(Br)Br.C[O:6][C:7]1[CH:12]=[CH:11][C:10]([F:13])=[CH:9][C:8]=1[O:14]C.C(O)C>C(Cl)Cl>[OH:6][C:7]1[CH:12]=[CH:11][C:10]([F:13])=[CH:9][C:8]=1[OH:14]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 702EthanolHCID 25134Boron tribromideHCID 5936404-Fluoro-1,2-dimethoxybenzene

生成物 1

HCID 1604584-Fluoro-1,2-benzenediol収率 104.1%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

A 1 M solution of boron tribromide in methylene chloride (500 mL, 0.50 mole) was cooled to -78 ° C. To this solution was added in a dropwise manner a solution of 46 g (0.30 mole) of 1,2-dimethoxy-4-fluorobenzene in 100 mL of methylene chloride. Upon completion of addition, the mixture was allowed to warm to ambient temperature at which it stirred for about 16 hours. At the conclusion of this period the reaction mixture was cooled to 0° C., and ethanol was added to the reaction mixture. The solvents were evaporated under reduced pressure, leaving 40 g of 1,2-dihydroxy-4-fluorobenzene as a residue. The NMR spectrum was consistent with the proposed structure.

後処理

  1. additionUpon completion of addition
  2. temperatureAt the conclusion of this period the reaction mixture was cooled to 0° C.
  3. customThe solvents were evaporated under reduced pressure

出典と根拠

ORDレコード
ord-c5d91d7d367342f6bd1ab91b35583ba7
出典データセット
uspto-grants-1994_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05346881

反応ノート

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