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

HRID 1247455
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HRID 1247455 반응식
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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1118Sulfuric AcidHCID 21907549Methyl 6-amino-3-bromo-2-methylbenzoateHCID 23668193Sodium Nitrite

생성물 1

HCID 21907510Methyl 3-bromo-6-hydroxy-2-methylbenzoate수율 86.6%

시약·촉매·용매 1

HCID 962Water용매3회

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온도
0 °C
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실험 절차

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)−.

후처리

  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

출처 및 근거

ORD 기록
ord-1d6fc0828fe34583b04d0a2bd786395c
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07129260B2

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