تفاعل #1442505

ord-82941e29a007470383d58c4e5f3c2e1c

معادلة التفاعل

C=CCCO
3-buten-1-ol
Cc1ccc(S(=O)(=O)Cl)cc1
Tosyl chloride
C=CCCO.Cc1ccc(S(=O)(=O)[O-])cc1
3-buten-1-ol 4-methylbenzene sulfonate
المردود 141.3%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصextracted with 60 mL diethyl ether
  2. 2
    تجفيفdried overnight in the freezer over MgSO4
  3. 3
    ترشيحThe mixture was filtered
  4. 4
    أخرىthe ether evaporated

الإجراء التجريبي

A solution of 3 g (42 mmol) 3-buten-1-ol in 10 mL dry pyridine was cooled in an ice bath. Tosyl chloride (7.9 g, 42 mmol), was added. After stirring for 3 h the mixture was poured into 30 mL of an ice/concentrated HCl 4/1 v/v solution, extracted with 60 mL diethyl ether and dried overnight in the freezer over MgSO4. The mixture was filtered and the ether evaporated to yield 7.22 g (76%) of 3-buten-1-ol 4-methylbenzene sulfonate as a yellow oil. 1H NMR (CDCl3): δ 2.39-2.53 (m, 2H, J=6.5 and 6.9 Hz, CH2—CH═CH2; and s, 3H, CH3—Ar), 4.08 (t, J=6.5 Hz, 2H, CH2OSO2), 5.09-5.15 (m, 2H, JZ═10.4, JE=16.6, Jgem=3.1 Hz, CH2—CH═CH2), 5.57-5.82 (m, 1H, JZ=10.4, JE=16.6, J =6.9 Hz, CH2—CH═CH2), 7.38 and 7.72 (d, 4H, J=8.6 Hz, Ar).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06586207B2uspto-grants-2003_07