反応 #43437

反応方程式

2-Methyl-2-propanethiol sodium salt

(4-[(phenylmethyl)oxy]-5-{[(trifluoromethyl)sulfonyl]oxy}-2-pyridinyl)methyl acetate

(R)-(+)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl

→

(5-[(1,1-Dimethylethyl)thio]-4-[(phenylmethyl)oxy]-2-pyridinyl}methyl acetate

溶媒

toluene

反応条件

後処理

1. 1
   その他The reaction mixture was purged with argon
2. 2
   その他the reaction mixture was flushed again with argon
3. 3
   温度then cooled
4. 4
   その他The solvent was evaporated
5. 5
   その他The residue was partitioned between a 1:1 mixture of water and EtOAc
6. 6
   その他The organic layer was separated
7. 7
   洗浄washed with brine
8. 8
   乾燥dried over magnesium sulphate
9. 9
   ろ過filtered through Kieselguhr
10. 10
    その他The residue was chromatographed
11. 11
    洗浄eluting with s 4:1 mixture of hexane

実験手順

To a solution of (4-[(phenylmethyl)oxy]-5-{[(trifluoromethyl)sulfonyl]oxy}-2-pyridinyl)methyl acetate (12.15 g, 30 mmol) in toluene (500 ml) was added (R)-(+)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (1.87 g, 3 mmol). The reaction mixture was purged with argon. Palladium acetate (663 mg, 3 mmol) was added and the mixture was stirred for 10 minutes. 2-Methyl-2-propanethiol sodium salt (4.69, 41.8 mmol) was added and the reaction mixture was flushed again with argon then heated to 80° C. for 7 hours then cooled. The solvent was evaporated. The residue was partitioned between a 1:1 mixture of water and EtOAc. The organic layer was separated and washed with brine, dried over magnesium sulphate and filtered through Kieselguhr. The residue was chromatographed eluting with s 4:1 mixture of hexane:EtOAc affording the product (8.3 g, 80%).

出典