تفاعل #9404

ord-fcacfd8cbe564e93b9260f019b289944

معادلة التفاعل

COc1ccc(C=O)c(O)c1O
21
COc1ccc(C=O)c(O)c1O
2, 3-dihydroxy-4-methoxybenzaldehyde
O=C([O-])[O-].[K+].[K+]
K2CO3
O
Water
CCOC(C)=O
EtOAc
CC(C)Br
2-bromopropane
COc1ccc(C=O)c(OC(C)C)c1OC(C)C
aldehyde
المردود 82.0%
COc1ccc(C=O)c(OC(C)C)c1OC(C)C
2,3-diisopropoxy-4-methoxybenzaldehyde
المردود 82.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
90°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةheated
  2. 2
    أخرىthe phases were separated
  3. 3
    استخلاصthe aqueous phase was extracted with EtOAc (3×200 mL)
  4. 4
    تجفيفThe combined organic solutions were dried over MgSO4
  5. 5
    تركيزconcentrated under reduced pressure
  6. 6
    أخرىPurification
  7. 7
    غسيلby flash column chromatography (silica gel, elution with hexane)

الإجراء التجريبي

To a solution of 21 (26.70 g, 158.7 mmol) in DMF (150 mL) under nitrogen, was added K2CO3 (65.84 g, 476.3 mmol) followed by 2-bromopropane (44.72 mL, 476.3 mmol) and heated to reflux (90° C.) for 12 hours. Water (200 mL) and EtOAc (200 mL) were added to the reaction mixture, the phases were separated, and the aqueous phase was extracted with EtOAc (3×200 mL). The combined organic solutions were dried over MgSO4 and concentrated under reduced pressure. Purification by flash column chromatography (silica gel, elution with hexane) provided 32.85 g (1.30.2 mmol, 82%) of the diusopropyl-protected aldehyde 22 as a yellow oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07091240B2uspto-grants-2006_08