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Hydroquinone → Propane, 1,3-bis(ethenylsulfonyl)-

HRID 258787
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HRID 258787 반응식
Cl[CH2:2][CH2:3][S:4]([CH2:7][CH2:8][CH2:9][S:10]([CH2:13][CH2:14]Cl)(=[O:12])=[O:11])(=[O:6])=[O:5].C1(C=CC(O)=CC=1)O.C(N(CC)CC)C>C(OCC)(=O)C>[CH:13]([S:10]([CH2:9][CH2:8][CH2:7][S:4]([CH:3]=[CH2:2])(=[O:6])=[O:5])(=[O:12])=[O:11])=[CH2:14]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 785HydroquinoneHCID 8471TriethylamineHCID 21424250HCID 21424250, 화합물

생성물 1

HCID 5072300Propane, 1,3-bis(ethenylsulfonyl)-

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

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온도
25 °C

실험 절차

1,3-Bis(2-chloroethylsulfonyl)propane (74.5 g., 0.249 mole) was suspended in 2,300 ml. of ethyl acetate containing 0.12 g. hydroquinone. Triethylamine (50.7 g., 0.50 mole) was dropped in with stirring, within 10 minutes at 25° C. The resulting mixture was stirred at 25° C. for 20 hours. The amine salt was filtered off and the ethyl acetate solution evaporated at 30° C. The tan-colored solid was washed with water, then recrystallized from ethanol; yield 32.8 g. (59 percent); m.p. 60°-63° C.

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후처리

  1. stirringThe resulting mixture was stirred at 25° C. for 20 hours
  2. filtrationThe amine salt was filtered off
  3. customthe ethyl acetate solution evaporated at 30° C
  4. washThe tan-colored solid was washed with water
  5. customrecrystallized from ethanol

출처 및 근거

ORD 기록
ord-05f74795aa924f489d8c2fbce9c07bfb
출처 데이터셋
uspto-grants-1977_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
USRE029305

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