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Methanesulfonyl chloride → Propanoic acid, 2-[(methylsulfonyl)oxy]-, ethyl ester, (R)-

HRID 1487179
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HRID 1487179 반응식
[OH:1][C@H:2]([CH3:8])[C:3]([O:5][CH2:6][CH3:7])=[O:4].[CH3:9][S:10](Cl)(=[O:12])=[O:11]>C1COCC1>[CH3:9][S:10]([O:1][C@H:2]([CH3:8])[C:3]([O:5][CH2:6][CH3:7])=[O:4])(=[O:12])=[O:11]
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참가 물질

4

반응물 2

HCID 31297Methanesulfonyl chlorideHCID 637513ethyl (2R)-2-hydroxypropanoate

생성물 1

HCID 2723759Propanoic acid, 2-[(methylsulfonyl)oxy]-, ethyl ester, (R)-수율 60.2%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
12.5 °C

실험 절차

(R)-ethyl 2-hydroxypropanoate (15 g, 0.127 mol) and TEA (15.4 g, 0.15 mol) were added to THF and then cooled to 10-15° C. Then MsCl (15 g, 0.13 mol) was added to the solution dropwise with cooling while maintaining the temperature in the range of 10-15° C. at about 2 hours. The mixture was allowed to warm to about 20° C. and the solid was filtered off. The solution was washed with water and dried, concentrated to afford (R)-ethyl 2-(methylsulfonyloxy)propanoate (15 g, 60%). 1H NMR (400 MHz, CDCl3) δ ppm, 5.11-5.14 (q, 1H), 4.24-4.29 (m, 2H), 2.81-3.17 (q, 3H, J=7.2 Hz), 1.61-1.43 (d, 3H, J=7.6 Hz), 1.30-1.32 (m, 3H).

후처리

  1. temperaturewith cooling
  2. temperaturewhile maintaining the temperature in the range of 10-15° C. at about 2 hours
  3. temperatureto warm to about 20° C.
  4. filtrationthe solid was filtered off
  5. washThe solution was washed with water
  6. customdried
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-05e472a86a05404490d5951d59894000
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09428508B2

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