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Diethanolamine hydrochloride → 1-(2-iso-Propoxytetrahydro-3-furanyl)-1,2-ethanediol

HRID 1692155
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HRID 1692155 반응식
[BH4-].[Na+].[OH:3][CH:4]([CH:10]1[CH2:14][CH2:13][O:12][CH:11]1[O:15][CH:16]([CH3:18])[CH3:17])[C:5](OCC)=[O:6].Cl.N(CCO)CCO>C(O)C.O>[CH:16]([O:15][CH:11]1[CH:10]([CH:4]([OH:3])[CH2:5][OH:6])[CH2:14][CH2:13][O:12]1)([CH3:18])[CH3:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 518946Diethanolamine hydrochlorideHCID 4311764Sodium borohydrideHCID 25242000Ethyl hydroxy-(2-isopropoxytetrahydro-3-furanyl)acetate

생성물 1

HCID 252420011-(2-iso-Propoxytetrahydro-3-furanyl)-1,2-ethanediol

시약·촉매·용매 2

HCID 702Ethanol용매2회HCID 962Water
용매

실험 절차

In a 2 L round bottom flask charged with 600 mL of ethanol and NaBH4 (12.55 g, 0.33 mol, 1.1 eq.) at 0° C., ethyl hydroxy-(2-isopropoxytetrahydro-3-furanyl)acetate (70 g, 0.3 mol, 1 eq.) dissolved in 400 mL of ethanol was added dropwise over 1 hour at 0° C. The mixture was allowed to warm up at room temperature and stirred for 19 hours. After cooling at 0° C., diethanolamine hydrochloride (46.7 g, 0.33 mol, 1.1 eq.) dissolved in 100 mL of water was added over 10 min. and stirred for 8 hours. The solvent was evaporated under reduced pressure to afford a clear yellow solid. After dilution with 300 mL of ethylacetate, the heterogeneous mixture was filtered over dicalite. The mixture was used directly in the next step.

후처리

  1. additionwas added dropwise over 1 hour at 0° C
  2. temperatureAfter cooling at 0° C.
  3. additionwas added over 10 min.
  4. stirringstirred for 8 hours
  5. customThe solvent was evaporated under reduced pressure
  6. customto afford a clear yellow solid
  7. filtrationAfter dilution with 300 mL of ethylacetate, the heterogeneous mixture was filtered over dicalite

출처 및 근거

ORD 기록
ord-b018d2d89a6b4f599925463454d95fb8
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08153829B2

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