تفاعل #1725

ord-25fc14e42f424677aa73d3c6c5b9ae9d

معادلة التفاعل

[Na+].[OH-]
sodium hydroxide
N#CCc1ccc(Oc2ccccc2)cc1
4-phenoxyphenylacetonitrile
C[Si](C)(C)N=[N+]=[N-]
trimethylsilylazide
CCC[CH2][Sn](=[O])[CH2]CCC
dibutyltin oxide
c1ccc(Oc2ccc(Cc3nnn[nH]3)cc2)cc1
5-(4-phenoxyphenylmethyl)-1H-tetrazole

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe mixture was heated
  2. 2
    درجة الحرارةto reflux for 19 hours
  3. 3
    غسيلwashed with diethyl ether (3×50 ml)
  4. 4
    غسيلthen washed with 5:1 ethyl acetate/tetrahydrofuran (60 ml) and ethyl acetate (2×50 ml)
  5. 5
    تجفيفThe combined organic layer was dried over anhydrous sodium sulfate
  6. 6
    ترشيحfiltered
  7. 7
    أخرىevaporated

الإجراء التجريبي

To a solution of 4-phenoxyphenylacetonitrile (1.16 g) in anhydrous toluene (30 ml) was added trimethylsilylazide (1.1 ml) and dibutyltin oxide (0.19 g). The mixture was heated to reflux for 19 hours then allowed to cool to room temperature. The reaction mixture was then added to 1M sodium hydroxide (100 ml) and washed with diethyl ether (3×50 ml). The aqueous layer was acidified with concentrated hydrochloric acid (30 ml) then washed with 5:1 ethyl acetate/tetrahydrofuran (60 ml) and ethyl acetate (2×50 ml). The combined organic layer was dried over anhydrous sodium sulfate, filtered and evaporated to give 5-(4-phenoxyphenylmethyl)-1H-tetrazole as a white solid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05726195uspto-grants-1998_03