تفاعل #1244264

ord-9d06994532b344cba44c54d3aba6899e

معادلة التفاعل

Cc1ccc(S(=O)(=O)OCC2COC(C)(C)O2)cc1
(2,2-dimethyl-1,3-dioxolan-4-yl)methyl 4-methylbenzenesulfonate
[N-]=[N+]=[N-].[Na+]
sodium azide
CC1(C)OCC(CN=[N+]=[N-])O1
13
المردود 76.0%
CC1(C)OCC(CN=[N+]=[N-])O1
4-(Azidomethyl)-2,2-dimethyl-1,3-dioxolane
المردود 76.0%

المذيبات

ظروف التفاعل

درجة الحرارة
80°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe solvent was evaporated under reduced pressure
  2. 2
    workup.ADDITIONdiluted with water (100 mL)
  3. 3
    استخلاصextracted 3 times with ethyl acetate (3×75 mL), which
  4. 4
    غسيلwas consecutively washed with H2O (100 mL), brine (100 mL)
  5. 5
    تجفيفfinally dried over MgSO4
  6. 6
    أخرىThe solvent was removed under vacuum

الإجراء التجريبي

To a solution of (2,2-dimethyl-1,3-dioxolan-4-yl)methyl 4-methylbenzenesulfonate (5.73 g, 20.00 mmol) in DMF (40 mL) was added sodium azide (2.6 g, 40.00 mmol) and the reaction mixture was stirred at 80° C. for 18 hr. The solvent was evaporated under reduced pressure, diluted with water (100 mL) and extracted 3 times with ethyl acetate (3×75 mL), which was consecutively washed with H2O (100 mL), brine (100 mL) and finally dried over MgSO4. The solvent was removed under vacuum to afford 2.2 g of 13 as brown oil (76% yield). 1H NMR (CDCl3, 400 MHz) δ: 4.21-4.27 (m, 1H), 4.02 (dd, J=6.4, 8.4 Hz, 1H), 3.74 (dd, J=6.0, 8.4 Hz, 1H), 3.36 (dd, J=4.8, 12.8 Hz, 1H), 3.26 (dd, J=5.6, 12.8 Hz, 1H), 1.43 (s, 3H), 1.33 (s, 3H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07807394B2uspto-grants-2010_10