تفاعل #8803

ord-16b875041d6e42ef88af956f49470849

معادلة التفاعل

NS(=O)(=O)c1cccc2ccccc12
1-naphthalene sulfonamide
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CCOC(=O)Cl
Ethyl chloroformate
CCOC(=O)NS(=O)(=O)c1cccc2ccccc12
ethyl 1-naphthylsulfonylcarbamate
المردود 67.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةwas heated
  2. 2
    درجة الحرارةunder reflux for 30 min
  3. 3
    درجة الحرارةthe resulting solution was heated
  4. 4
    درجة الحرارةunder reflux for 3 h
  5. 5
    درجة الحرارةThe mixture was cooled
  6. 6
    أخرىThe aqueous layer was collected
  7. 7
    workup.ADDITIONadjusted to pH 2 by addition of 1N HCl (aq)
  8. 8
    استخلاصExtraction with AcOEt (2×20 ml) and concentration of the dried organic extracts

الإجراء التجريبي

A mixture of 1-naphthalene sulfonamide (769 mg, 3.67 mmol) and potassium carbonate (563 mg, 4.07 mmol) in 2-butanone (9 ml) was heated under reflux for 30 min. Ethyl chloroformate (430 mg, 3.96 mmol) was added dropwise and the resulting solution was heated under reflux for 3 h. The mixture was cooled and diluted with H2O (30 ml) and AcOEt (10 ml). The aqueous layer was collected and adjusted to pH 2 by addition of 1N HCl (aq). Extraction with AcOEt (2×20 ml) and concentration of the dried organic extracts afforded ethyl 1-naphthylsulfonylcarbamate (674 mg, 67%) as a white solid. 1H NMR (DMSO-d6): δ 12.35 (bs, 1H), 8.57 (1H, d, J 8.6), 8.29 (2H, m), 8.11 (1H, d, J 7.7), 7.71 (3H, m), 3.90 (2H, q, J 7.1), 0.99 (3H, t, J 7.1).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07091209B2uspto-grants-2006_08