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1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 57443974, 화합물

HRID 500683
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HRID 500683 반응식
[CH2:1]([O:3][C:4]([C:6]1[S:10][C:9]2[CH:11]=[C:12]([CH2:15][OH:16])[CH:13]=[CH:14][C:8]=2[CH:7]=1)=[O:5])C.C1CCN2C(=NCCC2)CC1>CO>[CH3:1][O:3][C:4]([C:6]1[S:10][C:9]2[CH:11]=[C:12]([CH2:15][OH:16])[CH:13]=[CH:14][C:8]=2[CH:7]=1)=[O:5]
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참가 물질

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반응물 2

HCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 57443968HCID 57443968, 화합물

생성물 1

HCID 57443974HCID 57443974, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of 6-hydroxymethyl-benzo[b]thiophene-2-carboxylic acid ethyl ester (9.45 g, 40.0 mmol) and DBU (6.00 mL, 40.1 mmol) in anhydrous MeOH (200 mL) was allowed to stir for 2 d. After concentration, the residue was dissolved in EtOAc (800 mL) and washed with 1N HCl, water, saturated NaHCO3 and brine. The organic layer was dried, filtered and the filtrate was concentrated and dried to give 6-hydroxymethyl-benzo[b]thiophene-2-carboxylic acid methyl ester as off white solid. 1H NMR (CDCl3, 200 MHz) δ 8.03 (d, J=0.6 Hz, 1H), 7.90-7.80 (m, 2H), 7.39 (dd, J=8.0, 1.4 Hz, 1H), 4.83 (s, 2H), 3.94 (s, 3H), 1.98 (brs, 1H). MS (EI): cal'd 223.0 (MH+), exp 223.1 (MH+).

후처리

  1. concentrationAfter concentration
  2. dissolutionthe residue was dissolved in EtOAc (800 mL)
  3. washwashed with 1N HCl, water, saturated NaHCO3 and brine
  4. customThe organic layer was dried
  5. filtrationfiltered
  6. concentrationthe filtrate was concentrated
  7. customdried

출처 및 근거

ORD 기록
ord-4cf62c7da6d04569b5ceecf0920f92ea
출처 데이터셋
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07772238B2

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