تفاعل #2075683

ord-c1984557ff7442449f0ab413b2683a20

معادلة التفاعل

COc1ccc(C(Cl)(c2ccccc2)c2ccc(OC)cc2)cc1
4,4′-dimethoxytrityl chloride
CN(C)CC(O)CO
3-Dimethylamino-1,2-propanediol
COc1ccc(C(Cl)(c2ccccc2)c2ccc(OC)cc2)cc1
4,4′-Dimethoxytrityl chloride
COc1ccc(C(Cl)(c2ccccc2)c2ccc(OC)cc2)cc1
4,4′-dimethoxytrityl chloride
COc1ccc(C(OCC(O)CN(C)C)(c2ccccc2)c2ccc(OC)cc2)cc1
yellow gum
المردود 105.3%
COc1ccc(C(OCC(O)CN(C)C)(c2ccccc2)c2ccc(OC)cc2)cc1
1-(4,4′-Dimethoxytrityloxy)-3-dimethylamino-2-propanol
المردود 105.3%

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe flask was sealed
  2. 2
    أخرىflushed with argon
  3. 3
    workup.ADDITIONcharged with pyridine
  4. 4
    أخرىsealed
  5. 5
    أخرىto come to room temperature
  6. 6
    تركيزThe reaction was concentrated in vacuo
  7. 7
    workup.DISSOLUTIONre-dissolved in dichloromethane (300 mL)
  8. 8
    غسيلThe organic phase was washed with saturated bicarbonate (2×200 mL) and brine (1×200 mL)
  9. 9
    تجفيفdried over MgSO4
  10. 10
    ترشيحfiltered
  11. 11
    تركيزconcentrated
  12. 12
    أخرىdried under high vacuum

الإجراء التجريبي

3-Dimethylamino-1,2-propanediol (6.0 g, 50 mmol) was weighed into a 1 L round bottomed flask with a stir bar. The flask was sealed, flushed with argon, charged with pyridine and cooled to 0° C. 4,4′-Dimethoxytrityl chloride (17.9 g, 1.05 equiv.) was weighed into a 100 mL round bottomed flask, sealed and then dissolved in pyridine (80 mL). The 4,4′-dimethoxytrityl chloride solution was transferred to the stirring reaction mixture slowly, using additional fresh pyridine (20 mL) to effect the transfer of residual 4,4′-dimethoxytrityl chloride. The reaction was allowed to come to room temperature while stirring overnight. The reaction was concentrated in vacuo and re-dissolved in dichloromethane (300 mL). The organic phase was washed with saturated bicarbonate (2×200 mL) and brine (1×200 mL), dried over MgSO4, filtered, concentrated and dried under high vacuum to afford 22.19 g of a yellow gum that was used without further purification.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07641915B2uspto-grants-2010_01