تفاعل #155414

ord-62a5d83b7c594413a7da477ba5532a08

معادلة التفاعل

CC1CCCO1
2-methyltetrahydrofuran
Sc1cccc(S)c1
benzene-1,3-dithiol
CC1CCCO1
2-methyltetrahydrofuran
COS(=O)(=O)OC
dimethylsulfate
CC1CCCO1
2-methyltetrahydrofuran
[Na+].[OH-]
sodium hydroxide
CSc1cccc(S)c1
title compound
المردود 78.0%
CSc1cccc(S)c1
3-(Methylthio)benzenethiol
المردود 78.0%

المذيبات

ظروف التفاعل

درجة الحرارة
50°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe resulting solution was cooled to between 0° C. and 5° C.
  2. 2
    درجة الحرارةwise maintaining the temperature of the reaction mixture below 15° C.
  3. 3
    درجة الحرارةAfter cooling to ambient temperature the resulting solution
  4. 4
    أخرىthe phases were separated
  5. 5
    استخلاصThe organic phase was extracted with sodium hydroxide (2 M aqueous solution, 250 mL)
  6. 6
    درجة الحرارةthe combined aqueous phases were cooled to 10° C.
  7. 7
    workup.ADDITIONhydrochloric acid (6M aqueous solution, 500 mL) was added
  8. 8
    درجة الحرارةwhilst maintaining the temperature of the mixture below 25° C
  9. 9
    استخلاصThe resulting solution was extracted with tert-butylmethylether (2-fold 250 mL)
  10. 10
    غسيلthe combined organic phases were washed with water (500 mL)
  11. 11
    تركيزconcentrated in vacuo

الإجراء التجريبي

A solution of benzene-1,3-dithiol (50 g, 0.351 mmol) in 2-methyltetrahydrofuran (375 mL, 0.351 mmol) was treated with dimethylsulfate (33.3 mL, 0.351 mol) followed by 2-methyltetrahydrofuran (25 mL, used as line wash). The resulting solution was cooled to between 0° C. and 5° C. and sodium hydroxide (2M aqueous solution, 210.6 mL) was added drop wise maintaining the temperature of the reaction mixture below 15° C. followed by 2-methyltetrahydrofuran (25 mL, used as line wash) and heated under nitrogen to 50° C. for 4 hours. After cooling to ambient temperature the resulting solution was treated with tert-butylmethylether (500 mL) and the phases were separated. The organic phase was extracted with sodium hydroxide (2 M aqueous solution, 250 mL) and the combined aqueous phases were cooled to 10° C. and hydrochloric acid (6M aqueous solution, 500 mL) was added whilst maintaining the temperature of the mixture below 25° C. The resulting solution was extracted with tert-butylmethylether (2-fold 250 mL) and the combined organic phases were washed with water (500 mL) and concentrated in vacuo to give the title compound as a yellow oil, 78% yield, 42.9 g.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08822439B2uspto-grants-2014_09