تفاعل #1914819

ord-cd186954ca404a55bd09c2108542bbe0

معادلة التفاعل

OCC1COc2cscc2O1
(2,3-Dihydro-thieno[3,4-b][1,4]dioxin-2-yl)-methanol
[H-].[Na+]
NaH
O=S1(=O)CCCCO1
butanesultone
O=S(=O)([O-])CCCCOCC1COc2cscc2O1.[Na+]
4-(2,3-dihydro-thieno[3,4-b][1,4]dioxin-2-yl-methoxy)-butane-1-sulphonic acid sodium salt

المذيبات

ظروف التفاعل

درجة الحرارة
25°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةto reflux for 3 h
  2. 2
    أخرىthe solvent was removed
  3. 3
    workup.ADDITIONmethanol 5 was added
  4. 4
    workup.STIRRINGthe mixture was stirred
  5. 5
    ترشيحfiltered
  6. 6
    تركيزthe filtrate was concentrated
  7. 7
    workup.ADDITIONThe remaining oil was solidified by addition of hexane and ethanol
  8. 8
    workup.STIRRINGby stirring
  9. 9
    ترشيحFinal filtration
  10. 10
    أخرىdrying
  11. 11
    أخرىresulted in pure 4-(2,3-dihydro-thieno[3,4-b][1,4]dioxin-2-ylmethoxy)-butane-1-sulphonic acid sodium salt

الإجراء التجريبي

(2,3-Dihydro-thieno[3,4-b][1,4]dioxin-2-yl)-methanol (6.9 g, 40 mmol) was dissolved into tetrahydrofuran (100 mL) and blanketed by nitrogen. NaH (1.76 g) was added and stirring was continued for 30 min. Then butanesultone (6.0 g) was added dropwise after which the reaction mixture was brought to reflux for 3 h. Then it was cooled to 25° C. again, the solvent was removed, methanol 5 was added, the mixture was stirred, filtered and the filtrate was concentrated. The remaining oil was solidified by addition of hexane and ethanol, followed by stirring. Final filtration and drying resulted in pure 4-(2,3-dihydro-thieno[3,4-b][1,4]dioxin-2-ylmethoxy)-butane-1-sulphonic acid sodium salt as was demonstrated by NMR and mass spectroscopy.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07056600B2uspto-grants-2006_06