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Iodine → Methyl 3-iodo-4-methoxy-5-nitrobenzoate

HRID 852592
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HRID 852592 반응식
N[C:2]1[CH:3]=[C:4]([CH:9]=[C:10]([N+:14]([O-:16])=[O:15])[C:11]=1[O:12][CH3:13])[C:5]([O:7][CH3:8])=[O:6].[I:17]I.N(OC(C)(C)C)=O>C1(C)C=CC=CC=1>[I:17][C:2]1[CH:3]=[C:4]([CH:9]=[C:10]([N+:14]([O-:16])=[O:15])[C:11]=1[O:12][CH3:13])[C:5]([O:7][CH3:8])=[O:6]
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참가 물질

5

반응물 3

HCID 807IodineHCID 10906Tert-Butyl nitriteHCID 63022111Methyl 3-amino-4-(methyloxy)-5-nitrobenzoate

생성물 1

HCID 69356091Methyl 3-iodo-4-methoxy-5-nitrobenzoate수율 96.6%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

To a solution of methyl 3-amino-4-(methyloxy)-5-nitrobenzoate (D163) (370 mg, 1.64 mmol, 1 equiv) in toluene (20 ml) at 0° C. was added iodine (218 mg, 0.86 mmol, 0.5 equiv) then 1,1-dimethylethyl nitrite (200 mg, 1.75 mmol, 1.1 equiv) and the resulting mixture was stirred at room temperature for 15 h then partitioned between AcOEt and brine. The two layers were separated and the organic phase was dried over MgSO4 and concentrated in vacuo. Purification of the residue by flash chromatography on silica gel gave methyl 3-iodo-4-(methyloxy)-5-nitrobenzoate (D165) (280 mg, 51%) as a light brown solid. No molecular ion. RT=3.33 min.

후처리

  1. customthen partitioned between AcOEt and brine
  2. customThe two layers were separated
  3. dry with materialthe organic phase was dried over MgSO4
  4. concentrationconcentrated in vacuo
  5. customPurification of the residue by flash chromatography on silica gel

출처 및 근거

ORD 기록
ord-088853114f4744539a6364506dfee43c
출처 데이터셋
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07253198B2

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