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Hydrochloric Acid → HCID 59547213, 화합물

HRID 2408956
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HRID 2408956 반응식
[CH3:1][C:2]1[Se:6][C:5]([C:7]([O:9][CH3:10])=[O:8])=[CH:4][C:3]=1[N+:11]([O-])=O.Cl.[Cl-].[NH4+]>O.CO.[Fe]>[NH2:11][C:3]1[CH:4]=[C:5]([C:7]([O:9][CH3:10])=[O:8])[Se:6][C:2]=1[CH3:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 313Hydrochloric AcidHCID 25517Ammonium ChlorideHCID 59547210HCID 59547210, 화합물

생성물 1

HCID 59547213HCID 59547213, 화합물수율 79%

시약·촉매·용매 3

HCID 23925Iron촉매HCID 887Methanol용매
HCID 962
Water
용매

실험 절차

To a solution of methyl 5-methyl-4-nitroselenophene-2-carboxylate (2.3 g, 9.28 mmol) in a mixture of water (5 mL) and methanol (40 mL) was added conc. hydrochloric acid (1.0 mL). To the above solution was added iron powder (2.6 g, 46.4 mmol) followed by ammonium chloride (2.5 g, 46.4 mmol) at rt. The reaction mixture was refluxed for 1 h and was then allowed to cool to rt. The solution was filtered and basified with saturated sodium bicarbonate solution. The solution was extracted with ethyl acetate (4×100 mL) and the combined organic layer was dried over sodium sulfate and filtered. Solvent was evaporated and the residue was chromatographed over silica gel column using hexane-ethyl acetate (80:20) as eluent to give methyl 4-amino-5-methylselenophene-2-carboxylate (1.6 g, 79%), mp 66-68° C. 1H NMR (400 MHz, DMSO-d6): δ 7.57 (1H, s), 4.72 (2H, br s), 3.73 (3H, s), 2.24 (3H, s).

후처리

  1. temperatureThe reaction mixture was refluxed for 1 h
  2. filtrationThe solution was filtered
  3. extractionThe solution was extracted with ethyl acetate (4×100 mL)
  4. dry with materialthe combined organic layer was dried over sodium sulfate
  5. filtrationfiltered
  6. customSolvent was evaporated
  7. customthe residue was chromatographed over silica gel column

출처 및 근거

ORD 기록
ord-4e0fe5d4c4844ab3a2a94f1e61379192
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08815879B2

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