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Hydrochloric Acid → 5-(Dimethylamino)-N-(2-oxoethyl)naphthalene-1-sulfonamide

HRID 926233
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인쇄 미리보기

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HRID 926233 반응식
C[O:2][CH:3](OC)[CH2:4][NH:5][S:6]([C:9]1[C:18]2[C:13](=[C:14]([N:19]([CH3:21])[CH3:20])[CH:15]=[CH:16][CH:17]=2)[CH:12]=[CH:11][CH:10]=1)(=[O:8])=[O:7].Cl>CO>[O:2]=[CH:3][CH2:4][NH:5][S:6]([C:9]1[C:18]2[C:13](=[C:14]([N:19]([CH3:21])[CH3:20])[CH:15]=[CH:16][CH:17]=2)[CH:12]=[CH:11][CH:10]=1)(=[O:8])=[O:7]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 84426875HCID 84426875, 화합물

생성물 1

HCID 187021755-(Dimethylamino)-N-(2-oxoethyl)naphthalene-1-sulfonamide

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
25 °C

실험 절차

The acetal 11 (287 mg, 850 mop was dissolved in MeOH (1 mL) and coned HCl (0.5 mL) was added to the solution, which was stirred for 1 h at 25° C. The reaction mixture was then evaporated to dryness; the material left was dissolved in CH2Cl2 (10 mL) and the solution was washed with NaHCO3 (2 mL of a saturated aqueous solution). The organic layer was collected and was evaporated under low pressure to give the aldehyde as a light green foam, the total amount of which was used without further purification in the preparation of 12.

후처리

  1. customThe reaction mixture was then evaporated to dryness
  2. waitthe material left
  3. dissolutionwas dissolved in CH2Cl2 (10 mL)
  4. washthe solution was washed with NaHCO3 (2 mL of a saturated aqueous solution)
  5. customThe organic layer was collected
  6. customwas evaporated under low pressure

출처 및 근거

ORD 기록
ord-615ea1dead5a42e0b63008c3fd082021
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09284343B2

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