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Sodium borohydride → 1,3-Cyclopentanedimethanol

HRID 572911
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HRID 572911 반응식
[CH:1]1([CH:8]=[O:9])[CH2:5][CH2:4][CH:3]([CH:6]=[O:7])[CH2:2]1.[BH4-].[Na+]>O>[CH:1]1([CH2:8][OH:9])[CH2:5][CH2:4][CH:3]([CH2:6][OH:7])[CH2:2]1
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참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 14288766cyclopentane-1,3-dicarbaldehyde

생성물 1

HCID 5490561,3-Cyclopentanedimethanol

시약·촉매·용매 1

HCID 962Water용매

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온도
0 °C

실험 절차

To 1,3-cyclopentanedicarbaldehyde I-19 (1 equivalent) taken in a flask was added deoxygenated methanol. The reaction mixture was cooled to 0° C. and NaBH4 (2 equivalents) was added in small aliquots in order to avoid a raise in the reaction temperature above 10° C. The reaction mixture was left to warm to room temperature and stirred for an additional 3 h under nitrogen atmosphere. Distilled water was added to the reaction mixture to quench any remaining NaBH4 and then rotary evaporated to remove methanol from the solution. The remaining mixture was extracted with dichloromethane (5 times) and the combined organic fractions were dried over anhydrous sodium sulfate and evaporated to dryness to afford the title compound I-20.

후처리

  1. additionwas added
  2. customdeoxygenated methanol
  3. temperaturea raise in the reaction temperature above 10° C
  4. waitThe reaction mixture was left
  5. temperatureto warm to room temperature
  6. customto quench any remaining NaBH4
  7. customrotary evaporated
  8. customto remove methanol from the solution
  9. extractionThe remaining mixture was extracted with dichloromethane (5 times)
  10. dry with materialthe combined organic fractions were dried over anhydrous sodium sulfate
  11. customevaporated to dryness

출처 및 근거

ORD 기록
ord-07384d62d69240d795667736327bdce2
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09029531B2

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