Hydrochloric Acid → (2RS,3SR)-3-(2-Ethoxyphenoxy)-2-mesyloxy-3-phenyl-1-propanol

HRID 843378노트

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HRID 843378 반응식
[CH2:1]([O:3][C:4]1[CH:21]=[CH:20][CH:19]=[CH:18][C:5]=1[O:6][CH:7]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH:8]([OH:11])[CH2:9][OH:10])[CH3:2].C[Si](Cl)(C)C.[CH3:27][S:28](Cl)(=[O:30])=[O:29].Cl>C(OCC)(=O)C.C(N(CC)CC)C>[CH2:1]([O:3][C:4]1[CH:21]=[CH:20][CH:19]=[CH:18][C:5]=1[O:6][CH:7]([C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1)[CH:8]([O:11][S:28]([CH3:27])(=[O:30])=[O:29])[CH2:9][OH:10])[CH3:2]

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 6397ChlorotrimethylsilaneHCID 31297Methanesulfonyl chlorideHCID 13479304(2RS,3RS)-3-(2-Ethoxyphenoxy)-1,2-dihydroxy-3-phenylpropane

생성물 1

HCID 73084453(2RS,3SR)-3-(2-Ethoxyphenoxy)-2-mesyloxy-3-phenyl-1-propanol수율 102.9%

시약·촉매·용매 2

HCID 8471Triethylamine용매2회HCID 8857Ethyl Acetate용매3회

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온도
-17 °C

실험 절차

3-(2-Ethoxyphenoxy)-2-hydroxy-3-phenylpropanol from Example 2 (0.288 g, 1 mmole) and triethylamine ((0.15 mL, 1.1 mmole) were dissolved in ethyl acetate (5 mL) and cooled to −17° C. Trimethylsilyl chloride (0.13 mL, 1.0 mmole) dissolved in ethyl acetate (2 mL) was added over 10 minutes keeping the temperature below −15° C. a white precipitate formed during this addition. The mixture was stirred below −15° C. for 15 minutes. Triethylamine (0.15 mL, 1.1 mmole) was added, followed by methanesulfonyl chloride (0.085 mL, 1.1 mmole) dissolved ethyl acetate (2 mL) keeping the temperature below −15° C. The mixture was stirred below −15° C. for 15 minutes. Hydrochloric acid (2N, 2 mL) was added and the mixture was allowed to warm to 20-25° C. and stirred for 30 minutes. The phases were separated and the organic phase was washed with saturated aqueous sodium chloride solution (5 mL) and dried over sodium sulfate. The solution was evaporated to yield 0.377 g of an oil. The oil was chromatographed on silica (230-400 mesh) eluting with 1:1 hexane-ethyl acetate. The product-containing fractions were concentrated to yield 0.33 g (91%) of the title compound as an oil that solidified on standing; mp 83-86° C.; 1H NMR (400.13 MHZ, CDCl3) d 1.66 (t, J=8.2 Hz, 3H), 2.85 (s, 3H), 4.14-4.35 (m, 4H), 5,12 (m, 1H), 5.52 (d, J=6.1 Hz), 6.8-7.15 (m, 4H), 7.5-7.7 (m, 5H); 13C NMR (100.62 MHZ, CDCl3) d 14.73, 37.80, 62.19, 64.27, 81.40, 84.04, 112.88, 117.19, 120.67, 122.86, 127.40, 128.77, 128.86, 137.02, 146.40, 149.30; MS (ei ) m/e 366.

후처리

  1. additionwas added over 10 minutes
  2. customthe temperature below −15° C.
  3. customformed during this addition
  4. customthe temperature below −15° C
  5. stirringThe mixture was stirred below −15° C. for 15 minutes
  6. temperatureto warm to 20-25° C.
  7. stirringstirred for 30 minutes
  8. customThe phases were separated
  9. washthe organic phase was washed with saturated aqueous sodium chloride solution (5 mL)
  10. dry with materialdried over sodium sulfate
  11. customThe solution was evaporated

출처 및 근거

ORD 기록
ord-d656d570293e45c196a989092bf9f0c2
출처 데이터셋
uspto-grants-2002_04
특허 번호
US06376711B1

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