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Hydrogen Peroxide → 2-Fluoro-5-methoxyphenol

HRID 1161372
ノート
印刷プレビュー

反応式

HRID 1161372 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[CH:4][CH:3]=1.CN(CCN(CCN(C)C)C)C.C([Li])CCC.B(OC)(OC)[O:28]C.OO>O.C(O)(=O)C.C1COCC1>[F:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[CH:4][C:3]=1[OH:28]
参加物実験手順後処理出典と根拠反応ノート

参加物

9

反応物 5

HCID 784Hydrogen PeroxideHCID 8470Trimethyl borateHCID 99874-FluoroanisoleHCID 18196PentamethyldiethylenetriamineHCID 178418339Butyllithium

生成物 1

HCID 141189572-Fluoro-5-methoxyphenol

試薬・触媒・溶媒 3

HCID 176
Acetic Acid
溶媒
HCID 962Water溶媒
HCID 8028Tetrahydrofuran溶媒

実験手順

To a 200 ml THF solution containing 50.1 g of 1-fluoro-4-methoxybenzene and 70 g of N,N,N′,N′,N″-pentamethyldiethylenetriamine there was added dropwise 150 ml of n-butyllithium (2.66 M, hexane solution) over a period of 30 minutes, at −74° C. under a nitrogen atmosphere. After stirring for 3 hours at between −74° C. and −70° C., 100 ml of trimethyl borate was added. The temperature of the reaction mixture was then slowly allowed to rise to room temperature. Next, 70 ml of acetic acid and 75 ml of 30% aqueous hydrogen peroxide were added, and the reaction mixture was stirred overnight at room temperature. Water was then added to the reaction mixture, and then it was extracted with a mixture of hexane and ethyl acetate and dried over anhydrous magnesium sulfate. The desiccating agent was filtered off, and the filtrate was concentrated under reduced pressure to give a crude product of 1-fluoro-2-hydroxy-4-methoxybenzene (65.59 g) as a white solid.

後処理

  1. customat −74° C.
  2. customto rise to room temperature
  3. stirringthe reaction mixture was stirred overnight at room temperature
  4. extractionit was extracted with a mixture of hexane and ethyl acetate
  5. dry with materialdried over anhydrous magnesium sulfate
  6. filtrationThe desiccating agent was filtered off
  7. concentrationthe filtrate was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-ffc72892b9d84e258167541a9c0795d9
出典データセット
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07816522B2

反応ノート

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