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Chlorosulfonic acid → HCID 55279357, 화합물

HRID 467815
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HRID 467815 반응식
[Cl:1][S:2]([OH:5])(=O)=[O:3].[Cl:6][C:7]1[CH:12]=[CH:11][C:10]([CH2:13][CH3:14])=[CH:9][CH:8]=1>>[Cl:6][C:7]1[CH:12]=[CH:11][C:10]([CH2:13][CH3:14])=[CH:9][C:8]=1[S:2]([Cl:1])(=[O:5])=[O:3]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24638Chlorosulfonic acidHCID 693301-Chloro-4-ethylbenzene

생성물 1

HCID 55279357HCID 55279357, 화합물수율 22.9%

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온도
0 °C

실험 절차

Chlorosulfonic acid (4.0 mL, 59 mmol) was cooled to 0° C. and 1-chloro-4-ethylbenzene (1.0 mL, 7.5 mmol) was added dropwise over 30 min. The reaction mixture was stirred for 45 min at 0° C., poured with stirring onto 125 mL of crushed ice, and then extracted with ethyl acetate (2×100 mL). The ethyl acetate layers were combined, washed with water (100 mL), and dried over magnesium sulfate. The ethyl acetate was concentrated under reduced pressure to obtain an oil determined to be approximately a 1:1 mixture of isomers. This mixture was chromatographed on silica gel eluting with a hexane/ethyl acetate gradient to afford 0.41 g of the title compound. 1H NMR (CDCl3) δ 7.97 (s, 1H), 7.53 (d, 1H), 7.49 (d, 1H), 2.75 (q, 2H), 1.29 (t, 3H).

후처리

  1. additionpoured
  2. extractionextracted with ethyl acetate (2×100 mL)
  3. washwashed with water (100 mL)
  4. dry with materialdried over magnesium sulfate
  5. concentrationThe ethyl acetate was concentrated under reduced pressure
  6. customto obtain an oil
  7. additiona 1:1 mixture of isomers
  8. customThis mixture was chromatographed on silica gel eluting with a hexane/ethyl acetate gradient

출처 및 근거

ORD 기록
ord-dc75e3fdbae64d7398b7ca9618c14249
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08623890B2

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