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Chloroform → 1-oxoheptyl-D-allo-Threonine

HRID 52246
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HRID 52246 반응식
[C:1](Cl)(=[O:8])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7].[NH2:10][C@@H:11]([C:15]([OH:17])=[O:16])[C@@H:12]([CH3:14])[OH:13].[OH-].[Na+].C(Cl)(Cl)Cl>C1COCC1>[O:8]=[C:1]([NH:10][C@@H:11]([C:15]([OH:17])=[O:16])[C@@H:12]([CH3:14])[OH:13])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6212ChloroformHCID 14798Sodium HydroxideHCID 17313Heptanoyl chlorideHCID 90624D-Allothreonine

생성물 1

HCID 228516761-oxoheptyl-D-allo-Threonine

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A solution of n-heptanoyl chloride (440 mL, 2.83 mol) in THF (250 mL) is added dropwise, over a period of 30 min, to a cold (-5 to 0° C.), vigorously stirred mixture of D-allo-Thr (300 mg, 2.51 mmol) and 2N aq. NaOH (3.5 mL, 7.0 meq) in THF (4.0 mL). The resulting mixture is stirred for 2 h at the same temperature and overnight at room temperature. The volatiles are removed and the residue is diluted with water and acidified, using conc. HCl. The mixture is extracted with EtOAc and the combined organic solution is washed with brine, dried, filtered, and concentrated to provide crude 2c-1 (420 mg, containing 10% excess heptanoyl reagent) which solidifies upon standing. NMR δ1.28 (d, J=6.5, 3H), 4.20 (m, 1H), 4.61 (dd, J=3.4, 6.6, 1H), 6.56 (br d, J=6.9, 1H); [α]D26 -38±2 (CHCl3).

후처리

  1. customThe volatiles are removed
  2. additionthe residue is diluted with water
  3. extractionThe mixture is extracted with EtOAc
  4. washthe combined organic solution is washed with brine
  5. customdried
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customto provide crude
  9. addition2c-1 (420 mg, containing 10% excess heptanoyl reagent) which

출처 및 근거

ORD 기록
ord-d3cf16fae9814b7382521ff59c0352d6
출처 데이터셋
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05616612

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