Hydrochloric Acid → HCID 10858216, 화합물

HRID 2368892노트

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HRID 2368892 반응식
[CH3:1][C@H:2]([CH2:5][CH2:6][OH:7])[CH2:3][OH:4].C(N(CC)CC)C.[CH3:15][S:16](Cl)(=[O:18])=[O:17].Cl>C(Cl)Cl>[CH3:15][S:16]([O:4][CH2:3][C@H:2]([CH3:1])[CH2:5][CH2:6][O:7][S:16]([CH3:15])(=[O:18])=[O:17])(=[O:18])=[O:17]

참가 물질

6

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온도
-20 °C

실험 절차

To a solution of (R)-2-methylbutane-1,4-diol (30 g, 0.29 mol) in DCM (600 mL) was added triethylamine (100 mL, 0.72 mol). The solution was cooled to −20° C., and methanesulfonyl chloride (49 mL, 0.63 mol) was added dropwise over 30 min with vigorous stirring. The resulting mixture was stirred for additional 1 h while the temperature was maintained between −20 and −15° C. The mixture was allowed to warm to 0° C. and then poured into cold 1N HCl solution (100 mL). The organic layer was separated, and aqueous phase was extracted with DCM (100 mL). The combined organic extracts were washed with sat'd NaHCO3 solution, brine, dried over MgSO4, filtered and concentrated in vacuo. The resulting product (75.9 g, quant) was used directly for the next step. 1H NMR (400 MHz, CDCl3): δ 4.41-4.24 (m, 2H), 4.12 (dq, 2H), 3.02 (d, 6H), 2.13 (td, 1H), 1.95 (td, 1H), 1.80-1.65 (m, 1H), 1.07 (d, 3H).

후처리

  1. temperaturewas maintained between −20 and −15° C
  2. temperatureto warm to 0° C.
  3. customThe organic layer was separated
  4. extractionaqueous phase was extracted with DCM (100 mL)
  5. washThe combined organic extracts were washed with sat'd NaHCO3 solution, brine
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-636d96d909c940ce8e6ba19a359c1625
출처 데이터셋
uspto-grants-2014_04
특허 번호
US08703810B2

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