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Triethylamine → Methyl 3-Isocyanatothiophene-2-Carboxylate

HRID 1870532
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HRID 1870532 반응식
[O:1]=[C:2](Cl)OC(Cl)(Cl)Cl.[NH2:9][C:10]1[CH:14]=[CH:13][S:12][C:11]=1[C:15]([O:17][CH3:18])=[O:16].C(N(CC)CC)C>O1CCOCC1>[N:9]([C:10]1[CH:14]=[CH:13][S:12][C:11]=1[C:15]([O:17][CH3:18])=[O:16])=[C:2]=[O:1]
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참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 10426DiphosgeneHCID 89652Methyl 3-amino-2-thiophenecarboxylate

생성물 1

HCID 18696616Methyl 3-Isocyanatothiophene-2-Carboxylate

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

Diphosgene (4.6 mL) was added dropwise to a solution of methyl 3-amino-2-thiophenecarboxylate (5.0 g) in p-dioxane (100 mL) at room temperature under N2. Triethylamine (5.3 mL) was then added with concomitant formation of a white precipitate. The resulting reaction mixture was heated at reflux overnight. The reaction was allowed to cool to room temperature and then filtered to remove solid impurities. The precipitate was rinsed with diethyl ether (about 250 mL) and the filtrate was concentrated under reduced pressure to yield 6.4 g of crude title compound of Step A as a brown solid. 1H NMR (CDCl3): δ 7.43 (d,1H), 6.78 (d,1H), 3.92 (s,3H).

후처리

  1. customThe resulting reaction mixture
  2. temperaturewas heated
  3. temperatureat reflux overnight
  4. filtrationfiltered
  5. customto remove solid impurities
  6. washThe precipitate was rinsed with diethyl ether (about 250 mL)
  7. concentrationthe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-cfab7b1c4a6843019e0cb39045efbcef
출처 데이터셋
uspto-grants-2000_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06096895

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