تفاعل #969890

ord-52867257580c4af0bf082b8a3e028a37

معادلة التفاعل

CS(=O)(=O)Cl
methane sulfonyl chloride
CCc1ccc(CCO)nc1
2-(5-ethyl-pyridine-2-yl)-ethanol
CCN(CC)CC
triethylamine
CS(=O)(=O)Cl
methane sulfonyl chloride
CCc1ccc(CCOS(C)(=O)=O)nc1
title compound
CCc1ccc(CCOS(C)(=O)=O)nc1
Methanesulfonic acid 2-(5-ethyl-pyridin-2-yl)-ethyl ester

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGthe reaction stirred for 30 min
  2. 2
    غسيلwashed with H2O and brine
  3. 3
    تجفيفThe organic layer was dried (MgSO4)
  4. 4
    تركيزthe solution concentrated

الإجراء التجريبي

To a solution of 2-(5-ethyl-pyridine-2-yl)-ethanol (25.34 g) and triethylamine (46.7 mL) in DCM (130 mL) at 0° C. under nitrogen was added methane sulfonyl chloride (15.56 mL), then the reaction mixture was allowed to warm to room temperature and stirred overnight. A further portion of methane sulfonyl chloride (3.88 mL) was added and the reaction stirred for 30 min. The reaction was diluted with DCM and washed with H2O and brine. The organic layer was dried (MgSO4) and the solution concentrated to give the title compound as a red oil (38.24 g). 1H NMR (400 MHz, CDCl3): δ 8.39 (d, J=2.2 Hz, 1H), 7.47 (dd, J=7.7, 2.3 Hz, 1H), 7.14 (d, J=7.7 Hz, 1H), 4.64 (t, J=6.5 Hz, 2H), 3.19 (t, J=6.5 Hz, 2H), 2.90 (s, 3H), 2.64 (q, J=7.6 Hz, 2H), 1.25 (t, J=7.6 Hz, 3H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08236786B2uspto-grants-2012_08