반응 #10177

반응 방정식

β-ethoxyacrylic acid ethyl ester

2-bromobenzyl phenyl sulfone

tricyclohexylphophine

sodium tert-butoxide

potassium dihydrogen phosphate

→

3-benzenesulfonyl-3H-indene-1-carboxylic acid ethyl ester

수율 85.0%

용매

tetrahydrofuran

methyl tert-butyl ether

tetrahydrofuran

반응 조건

후처리

1. 1
   workup.ADDITIONUpon complete addition the reaction
2. 2
   온도was warmed to room temperature
3. 3
   온도heated to 60° C. for 2 hours
4. 4
   온도The reaction was cooled to room temperature
5. 5
   기타The aqueous layer was separated and saturated by addition of solid sodium chloride
6. 6
   추출extracted with ethyl acetate (2×50 mL)
7. 7
   기타The organic layer was separated
8. 8
   세척washed twice with aqueous saturated sodium chloride (2×30 mL)
9. 9
   건조dried over sodium sulfate
10. 10
    여과filtered
11. 11
    농축concentrated in vacuo

실험 절차

A solution of tricyclohexylphophine (46 mg, 0.164 mmol) in tetrahydrofuran (2.5 mL) under nitrogen was charged with palladium (II) acetate (24.5mg, 0.109 mmol). The reaction mixture was stirred for 45 minutes, then cooled to 0° C. and charged with sodium tert-butoxide (270 mg, 2.73 mmol). After 5 minutes a solution of β-ethoxyacrylic acid ethyl ester (158 μL, 1.09 mmol) and 2-bromobenzyl phenyl sulfone (340 mg, 1.09 mmol) in tetrahydrofuran (2.5 mL) was added dropwise over 2 minutes. Upon complete addition the reaction was warmed to room temperature and then heated to 60° C. for 2 hours. The reaction was cooled to room temperature, then diluted with methyl tert-butyl ether (25 mL) and poured into aqueous potassium dihydrogen phosphate (0.25 M, 25 mL), pH=7. The aqueous layer was separated and saturated by addition of solid sodium chloride and extracted with ethyl acetate (2×50 mL). The organic layer was separated and washed twice with aqueous saturated sodium chloride (2×30 mL), dried over sodium sulfate, filtered and concentrated in vacuo affording 3-benzenesulfonyl-3H-indene-1-carboxylic acid ethyl ester as a light orange oil (304 mg, 0.925 mmol, 85%). 1H NMR (400 MHz, CDCl3) δ 7.88–7.86 (m, 1H), 7.75–7.72 (m, 1H), 7.49–7.43 (m, 3H), 7.36–7.32 (m, 2H), 7.27–7.25 (m, 3H), 5.15 (d, 1H, J=2.1), 4.27 (q, 2H, J=7.1), 1.34 (t, 3H, J=7.1); IR (ATR, neat) 1709, 1649, 1463, 1444, 1314, 1271, 1247, 1188, 1133, 1081, 1044, 773, 752, 722, 686, 575, 528.

출처