تفاعل #220091

ord-9802d73f1a3b4785b54a8635b7bf0fd4

معادلة التفاعل

O=C([O-])[O-].[K+].[K+]
Potassium carbonate
Cl.O.O=C1CCNCC1
4-piperidone monohydrate hydrochloride
CS(=O)(=O)Cl
methylsulfonyl chloride
CS(=O)(=O)N1CCC(=O)CC1
white solid
المردود 87.1%
CS(=O)(=O)N1CCC(=O)CC1
1-Methanesulfonyl-piperidin-4-one
المردود 87.1%

المذيبات

ظروف التفاعل

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

المعالجة

  1. 1
    أخرىwas partitioned between CH2Cl2 (500 mL) and saturated aqueous NaHCO3 (500 mL)
  2. 2
    استخلاصThe aqueous layer was extracted with CH2Cl2 (3×200 mL)
  3. 3
    غسيلThe organic layer was washed with 1% KHSO4 (250 mL)
  4. 4
    تجفيفdried (Na2SO4)
  5. 5
    تركيزconcentrated

الإجراء التجريبي

Potassium carbonate (324 g, 2340 mmol) was added to a solution of 4-piperidone monohydrate hydrochloride (90 g, 586 mmol) in chloroform (300 mL) and water (300 mL). The slurry was cooled to 0° C. and treated with methylsulfonyl chloride (136 mL, 1760 mmol) by dropwise addition over a 1 h period (gas evolution was observed). The reaction mixture was allowed to shake for 72 h and was partitioned between CH2Cl2 (500 mL) and saturated aqueous NaHCO3 (500 mL). The aqueous layer was extracted with CH2Cl2 (3×200 mL). The organic layer was washed with 1% KHSO4 (250 mL), dried (Na2SO4), and concentrated to afford 90.5 g (87%) of a white solid. MS (electrospray): exact mass calculated for C6H11NO3S, 177.1; m/z found, 178.1 [M+H]+. HPLC (reverse phase conditions): tR=2.19 min. 1H NMR (400 MHz, CDCl3): 3.60 (t, J=6.5 Hz, 4H), 2.89 (s, 3H), 2.59 (t, J=6.3 Hz, 4H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07388011B2uspto-grants-2008_06