反応 #2358524

ord-0e4f4e4a4e7f4d82a5a8aa1541f20587

反応方程式

BrCCBr
1.2-dibromoethane
CC(C)(C)OC(=O)NCCO
boc-glycinol
N#N
N2
CCOC(=O)/N=N/C(=O)OCC
DEAD
CS(=O)(=O)c1cc(O)cc(F)c1
3-fluoro-5-methylsulfonyl-phenol
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
CC(C)(C)OC(=O)NCCOc1cc(F)cc(S(C)(=O)=O)c1
title compound
収率 70.0%
CC(C)(C)OC(=O)NCCOc1cc(F)cc(S(C)(=O)=O)c1
tert-butyl 2-[3-fluoro-5-(methylsulfonyl)phenoxy]ethyl-carbamate
収率 70.0%

反応条件

温度
70°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度cooled to room temperature
  2. 2
    抽出The aqueous phase was extracted with ethyl acetate (2×100 ml)
  3. 3
    洗浄The combined organic phase was washed with aqueous NaOH (3 M, 50 ml) and brine (75 ml)
  4. 4
    乾燥dried (Na2SO4)
  5. 5
    その他evaporated
  6. 6
    その他Purification by flash column chromatography (ethyl acetate/isooctane, 0:1 to 1:0)

実験手順

A mixture of triphenylphosphine (1.9 g, 7.3 mmol) in dry THF (20 ml) was flushed with N2(g) and DEAD (3.1 ml, 6.9 mmol) was added drop-wise, 1.2-dibromoethane followed by 3-fluoro-5-methylsulfonyl-phenol (1.1 g, 6.1 mmol) and then boc-glycinol (1.0 ml, 6.1 mmol) in portions. The mixture was stirred at 70° C. for 20 h, cooled to room temperature and water and EtOAc was added. The aqueous phase was extracted with ethyl acetate (2×100 ml). The combined organic phase was washed with aqueous NaOH (3 M, 50 ml) and brine (75 ml), dried (Na2SO4) and evaporated. Purification by flash column chromatography (ethyl acetate/isooctane, 0:1 to 1:0) gave the title compound (1.4 g, 70%). MS m/z (relative intensity, 70 eV 298 (M+, 18), 296 (M+, 18), 109 (bp), 107 (99), 82 (15).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09120728B2uspto-grants-2015_09