Dimethyl Sulfoxide → (S)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-2-oxo-oxazolidine-5-carbaldehyde

HRID 1640520노트

반응식

HRID 1640520 반응식
C(Cl)(=O)C(Cl)=O.CS(C)=O.[O:11]1[C:16]2[CH:17]=[CH:18][C:19]([N:21]3[CH2:25][C@@H:24]([CH2:26][OH:27])[O:23][C:22]3=[O:28])=[CH:20][C:15]=2[O:14][CH2:13][CH2:12]1>C(Cl)Cl>[O:11]1[C:16]2[CH:17]=[CH:18][C:19]([N:21]3[CH2:25][C@@H:24]([CH:26]=[O:27])[O:23][C:22]3=[O:28])=[CH:20][C:15]=2[O:14][CH2:13][CH2:12]1

참가 물질

5

반응 조건

온도
0 °C

실험 절차

A solution of oxalyl chloride (0.229 mL, 2.71 mmol) in DCM (5 mL) was cooled to −78° C. and DMSO (0.395 mL, 5.572 mmol) was added dropwise. The mixture was stirred for 10 min at that temperature and a suspension of (S)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-5-hydroxymethyl-oxazolidin-2-one (400 mg, 1.59 mmol) in DCM (6 mL) was then added dropwise within 1 min. Stirring was continued for 20 min. TEA (0.665 mL, 4.78 mmol) was added and the mixture was stirred for 5 min, and then allowed to warm to 0° C. The mixture was filtered through Celite and concentrated with a bath temperature below 30° C. The residue was partitioned between water and EA and the org. layer was washed with brine, dried over Na2SO4 and concentrated with a bath temperature below 30° C. The highly unstable intermediate was used immediately in the next step.

후처리

  1. additionwas then added dropwise within 1 min
  2. stirringStirring
  3. waitwas continued for 20 min
  4. stirringthe mixture was stirred for 5 min
  5. filtrationThe mixture was filtered through Celite
  6. concentrationconcentrated with a bath temperature below 30° C
  7. customThe residue was partitioned between water and EA
  8. washlayer was washed with brine
  9. dry with materialdried over Na2SO4
  10. concentrationconcentrated with a bath temperature below 30° C

출처 및 근거

ORD 기록
ord-98ad07b8ad1a4051819ffc4a41c2b23c
출처 데이터셋
uspto-grants-2012_02
특허 번호
US08114867B2

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