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Sodium borohydride → 4-Chloro-2,6-dimethylbenzyl alcohol

HRID 1016446
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HRID 1016446 반응식
[Cl:1][C:2]1[CH:9]=[C:8]([CH3:10])[C:5]([CH:6]=[O:7])=[C:4]([CH3:11])[CH:3]=1.[BH4-].[Na+]>CO>[Cl:1][C:2]1[CH:3]=[C:4]([CH3:11])[C:5]([CH2:6][OH:7])=[C:8]([CH3:10])[CH:9]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 184069754-Chloro-2,6-dimethylbenzaldehyde

생성물 1

HCID 695457014-Chloro-2,6-dimethylbenzyl alcohol

시약·촉매·용매 1

HCID 887Methanol용매

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온도
0 °C

실험 절차

Dissolve 4-chloro-2,6-dimethyl benzaldehyde (5.0 g, 168.64 g/mol) in 100 mL dry MeOH. Cool to 0° C. while stirring under N2. Portionwise add powdered NaBH4 (0.76 g, 37.85 g/mol) over 5 min. Stir at 0° C. for 2 h, monitoring by TLC until aldehyde consumed, then evaporate to a yellow oil. Add H2O (50 mL) and bring to pH 7.0 by addition of saturated NH4Cl. Extract the neutral aqueous layer with CH2Cl2 (3×75 mL) and dry the pooled organic layers over Na2SO4. Filter and concentrate to a yellow oil. Flush through a pad of silica to remove baseline material, then evaporate to a yellow solid (3.0 g) which can be used without further purification. LCMS=171.6 (MH+), 169.6 (M−).

후처리

  1. stirringStir at 0° C. for 2 h
  2. custommonitoring by TLC until aldehyde consumed
  3. customevaporate to a yellow oil
  4. additionAdd H2O (50 mL) and bring to pH 7.0 by addition of saturated NH4Cl
  5. extractionExtract the neutral aqueous layer with CH2Cl2 (3×75 mL)
  6. dry with materialdry the pooled organic layers over Na2SO4
  7. filtrationFilter
  8. concentrationconcentrate to a yellow oil
  9. customFlush through a pad of silica
  10. customto remove baseline material
  11. customevaporate to a yellow solid (3.0 g) which
  12. customcan be used without further purification

출처 및 근거

ORD 기록
ord-4d8a3256ddf647b881ebd1bce13721a3
출처 데이터셋
uspto-grants-2002_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06476038B1

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