反応 #1265376

反応方程式

n-BuLi

tetrahydrofurane

Acetonitrile

lithium acetonitrile

NaOH

Isobutylene sulfide

THF

→

product 7

収率 39.0%

4-Mercapto-4-methylpentanoic acid

収率 39.0%

溶媒

Ethanol

water

water

反応条件

後処理

1. 1
   その他A 500 mL flask was equipped with a stir bar and a 150 mL addition funnel
2. 2
   その他was formed
3. 3
   workup.ADDITIONadded drop wise over approximately 30 min via the addition funnel
4. 4
   その他The cooling bath was removed
5. 5
   温度The flask was cooled in an ice/water bath as 38 mL of 0.5 M HCl
6. 6
   workup.ADDITIONwas added drop-wise
7. 7
   洗浄the aqueous layer was washed twice with 75 mL of ethyl acetate
8. 8
   乾燥dried over approximately 20 g of anhydrous sodium sulfate
9. 9
   その他transferred to a 250 mL flask
10. 10
    その他Solvent was removed by rotary evaporation under vacuum
11. 11
    その他to give crude 6
12. 12
    workup.ADDITIONwas slowly added
13. 13
    その他The flask was equipped with a reflux condenser
14. 14
    温度The reaction was refluxed overnight
15. 15
    温度then cooled to room temperature
16. 16
    抽出the mixture was extracted twice with 25 mL portions of a 2:1 mixture of ethyl acetate and hexane
17. 17
    抽出then extracted three times with 75 mL portions of ethyl acetate
18. 18
    乾燥The organic layers were dried over anhydrous Na2SO4 and solvent
19. 19
    その他was removed by rotary evaporation under vacuum

実験手順

A 500 mL flask was equipped with a stir bar and a 150 mL addition funnel. The system was placed under an argon atmosphere. 150 mL of anhydrous tetrahydrofurane (THBF) and 75 mL of 2.5 M n-BuLi in hexanes (18.7 mmol) were added via a canula and the solution was cooled in a −78° C. dry ice/acetone bath. Acetonitrile (7.3 g, 9.4 mL, 18 mmol) was added drop-wise via a syringe over approximately 5 min. The reaction was stirred for 30 min, while white lithium-acetonitrile precipitate was formed. Isobutylene sulfide (15 g, 17 mmol) was dissolved in 100 mL of anhydrous THF and added drop wise over approximately 30 min via the addition funnel. The cooling bath was removed and the reaction was allowed to stir for 3 hours. The flask was cooled in an ice/water bath as 38 mL of 0.5 M HCl was added drop-wise. The THF layer was retained and the aqueous layer was washed twice with 75 mL of ethyl acetate. The THF and ethyl acetate layers were combined, dried over approximately 20 g of anhydrous sodium sulfate and transferred to a 250 mL flask. Solvent was removed by rotary evaporation under vacuum to give crude 6. Ethanol (30 mL) and a stir bar were added. The contents were stirred as a solution of 8.0 g NaOH in 30 mL deionized water was slowly added. The flask was equipped with a reflux condenser and placed under an argon atmosphere. The reaction was refluxed overnight then cooled to room temperature. Deionized water (60 mL) was added and the mixture was extracted twice with 25 mL portions of a 2:1 mixture of ethyl acetate and hexane. The aqueous layer was acidified to pH 2 with concentrated HCl then extracted three times with 75 mL portions of ethyl acetate. The organic layers were dried over anhydrous Na2SO4 and solvent was removed by rotary evaporation under vacuum to give 10 g of product 7 (39% yield). Material was used without further purification. 1H NMR (CDCl3): δ1.38 (6H, s), 1.87-1.93 (2H, m), 2.08 (1H, s), 2.51-2.57 (2H, m).

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