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Methylamine → HCID 19756475, 화합물

HRID 1587883
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HRID 1587883 반응식
Br[CH2:2][CH2:3][C:4]1[CH:5]=[CH:6][C:7]2[O:11][CH2:10][CH2:9][C:8]=2[CH:12]=1.[CH3:13][NH2:14]>CO>[O:11]1[C:7]2[CH:6]=[CH:5][C:4]([CH2:3][CH2:2][NH:14][CH3:13])=[CH:12][C:8]=2[CH2:9][CH2:10]1
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참가 물질

4

반응물 2

HCID 6329MethylamineHCID 218311605-(2-Bromoethyl)-2,3-dihydro-1-benzofuran

생성물 1

HCID 19756475HCID 19756475, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of 5-(2-bromoethyl)-2,3-dihydrobenzofuran (1.5 g-see Preparation 20) in 33% methylamine in methanol (40 ml) was heated at 100° C. in a stainless steel pressure vessel for 6 hours then concentrated in vacuo. The residue was partitioned between dichloromethane (50 ml) and 10% aqueous sodium carbonate (50 ml). The layers were separated and the aqueous layer was further extracted with dichloromethane (2×50 ml). The aqueous layer was concentrated in vacuo to give a solid which was triturated with boiling 2-propanol. The mixture was filtered and the filtrate concentrated in vacuo to give a solid which was purified by column chromatography on silica eluting with dichloromethane containing methanol (0% up to 1%). The product-containing fractions were combined and concentrated in vacuo to give the title compound as a colourless solid, yield, 0.31 g, m.p. 153°-155° C.

후처리

  1. concentrationthen concentrated in vacuo
  2. customThe residue was partitioned between dichloromethane (50 ml) and 10% aqueous sodium carbonate (50 ml)
  3. customThe layers were separated
  4. extractionthe aqueous layer was further extracted with dichloromethane (2×50 ml)
  5. concentrationThe aqueous layer was concentrated in vacuo
  6. customto give a solid which
  7. customwas triturated with boiling 2-propanol
  8. filtrationThe mixture was filtered
  9. concentrationthe filtrate concentrated in vacuo
  10. customto give a solid which
  11. customwas purified by column chromatography on silica eluting with dichloromethane
  12. additioncontaining methanol (0% up to 1%)
  13. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-a39c5d29fb8342879d622b334d6f37d8
출처 데이터셋
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05219871

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