反应 #1355843

ord-453f4023b964490f8e1ef6d001a9b29f

反应方程式

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
收率 141.3%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    萃取extracted with 60 mL diethyl ether
  2. 2
    干燥dried overnight in the freezer over MgSO4
  3. 3
    过滤The mixture was filtered
  4. 4
    其他the ether evaporated

实验过程

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).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07198915B2uspto-grants-2007_04