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Sulfuric Acid → Methyl 3-bromo-6-hydroxy-2-methylbenzoate

HRID 1247455
ノート
印刷プレビュー

反応式

HRID 1247455 の反応式
N[C:2]1[C:7]([C:8]([O:10][CH3:11])=[O:9])=[C:6]([CH3:12])[C:5]([Br:13])=[CH:4][CH:3]=1.N([O-])=[O:15].[Na+].OS(O)(=O)=O>O>[Br:13][C:5]1[C:6]([CH3:12])=[C:7]([C:2]([OH:15])=[CH:3][CH:4]=1)[C:8]([O:10][CH3:11])=[O:9]
参加物反応条件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 1118Sulfuric AcidHCID 21907549Methyl 6-amino-3-bromo-2-methylbenzoateHCID 23668193Sodium Nitrite

生成物 1

HCID 21907510Methyl 3-bromo-6-hydroxy-2-methylbenzoate収率 86.6%

試薬・触媒・溶媒 1

HCID 962Water溶媒3 回

反応条件

温度
0 °C
このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

実験手順

A 0° C. suspension of Example 106A (1 g, 4.1 mmol) in water (6 mL) was treated dropwise with a solution of NaNO2 (285 mg) in water (1.25 mL), stirred at 0° C. for 15 minutes, then added slowly to a 90° C. solution of concentrated H2SO4 (4 mL) in water (4 mL). The reaction was stirred at 90° C. for 45 minutes, cooled to room temperature, and extracted three times with diethyl ether. The combined extracts were washed with aqueous NaHCO3 and brine, dried (MgSO4), filtered, and concentrated to give 0.87 g of the desired product. MS (ESI(−)) m/e 226 (M−H)−.

後処理

  1. stirringThe reaction was stirred at 90° C. for 45 minutes
  2. temperaturecooled to room temperature
  3. extractionextracted three times with diethyl ether
  4. washThe combined extracts were washed with aqueous NaHCO3 and brine
  5. dry with materialdried (MgSO4)
  6. filtrationfiltered
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-1d6fc0828fe34583b04d0a2bd786395c
出典データセット
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07129260B2

反応ノート

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