تفاعل #710538

ord-1d89b1c5bfaa418388eb4cba1eda6e74

معادلة التفاعل

CS(=O)(=O)Cl
methanesulfonyl chloride
OCc1ccc(Br)cc1
4-bromobenzylalcohol
CCN(CC)CC
Et3N
CS(=O)(=O)OCc1ccc(Br)cc1
methanesulfonic acid 4-bromo-benzyl ester
المردود 94.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىquenched with water
  2. 2
    workup.ADDITIONSaturated aqueous NaHCO3 was added
  3. 3
    استخلاصthe product was extracted with DCM
  4. 4
    ترشيحthe combined organic extracts were filtered through a phase separator cartridge
  5. 5
    تركيزconcentrated

الإجراء التجريبي

To a solution of 4-bromobenzylalcohol (2 g, 10.7 mmol) in DCM (30 mL) at 0° C. was added Et3N (2.2 mL, 16.0 mmol) followed by methanesulfonyl chloride (910 μL, 11.8 mmol). The reaction was allowed to warm to room temperature, stirred for 2 hours and then quenched with water. Saturated aqueous NaHCO3 was added, the product was extracted with DCM, the combined organic extracts were filtered through a phase separator cartridge and concentrated to give methanesulfonic acid 4-bromo-benzyl ester (2.67 g, 10 mmol, 94%). A solution of the crude product (2.67 g, 10 mmol) in DMSO (40 mL) was stirred at room temperature for 16 hours with potassium thioacetate (1.26 g, 11 mmol). The reaction was treated with water and extracted with DCM, filtered through a phase separator, concentrated and purified by silica gel column chromatography (0-50% DCM in cyclohexane) to give thioacetic acid S-(4-bromo-benzyl) ester (1.81 g, 7.39 mmol, 69%). 1H NMR (300 MHz, CDCl3): δ 7.41 (d, 2 H), 7.16 (d, 2 H), 4.05 (s, 2 H), 2.35 (s, 3 H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09302985B2uspto-grants-2016_04