反応 #639192

反応方程式

methanesulfonyl chloride

cholesterol

triethylamine

→

product

収率 99.0%

3β-Cholest-5-en-3-yl methanesulfonate

収率 99.0%

溶媒

CH2Cl2

CH2Cl2

反応条件

後処理

1. 1
   その他When the cholesterol was consumed
2. 2
   その他the solvent was removed in vacuo
3. 3
   workup.DISSOLUTIONThe resulting residue was redissolved in CH2Cl2 (15 mL)
4. 4
   その他the product was precipitated by addition of MeOH (150 mL)
5. 5
   ろ過the product collected by vacuum filtration
6. 6
   洗浄The solid was washed with MeOH (30 mL)
7. 7
   その他dried under vacuum

実験手順

A solution of cholesterol (19.3 g, 50.0 mmol) in anhydrous CH2Cl2 (250 mL) was cooled to 4° C. by ice-water bath. To this solution, triethylamine (13.9 mL, 100.0 mmol) was added, followed by the dropwise addition of methanesulfonyl chloride (4.3 mL, 55 mmol) in anhydrous CH2Cl2 (50 mL). The reaction was maintained at 4° C. and stirred for 3 h. When the cholesterol was consumed as analyzed by TLC (hexanes/ethyl acetate, 5:1), the solvent was removed in vacuo. The resulting residue was redissolved in CH2Cl2 (15 mL), the product was precipitated by addition of MeOH (150 mL), and the product collected by vacuum filtration. The solid was washed with MeOH (30 mL) and dried under vacuum to yield the product (23.0 g, 99.0%) as a white solid, mp 119-120° C.; 1H NMR (300 MHz, CDCl3) δ 5.41 (s, 1H), 4.56-4.45 (m, 1H), 3.00 (s, 3H), 2.57-2.43 (m, 2H), 2.04-0.81 (m, 38H), 0.67 (s, 3H); 13C NMR (75 MHz, CDCl3) δ 138.6, 123.7, 81.9, 56.5, 56.0, 49.9, 42.2, 39.6, 39.4, 39.1, 38.7, 36.8, 36.3, 36.1, 35.7, 31.8, 31.7, 28.9, 28.1, 27.9, 24.2, 23.8, 22.8, 22.5, 20.9, 19.1, 18.6, 11.8; IR (film) ν max 3029, 2944, 2908, 2861, 1468, 1440, 1415, 1353, 1330, 1173 cm−1; ESI+m/z ((MNa)+ 487.3237, C28H48O3SNa requires 487.3222).

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