반응 #710553

ord-b34281d7f1ce414bb232c03916051621

반응 방정식

CC(C)(C)OC(=O)NCC(=O)CO[Si](C)(C)C(C)(C)C
tert-butyl 3-(tert-butyldimethylsilyloxy)-2-oxopropylcarbamate
FC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.F[B-](F)(F)F
fluoromethyl(triphenyl)-phosphonium tetrafluoroborate
C[Si](C)(C)[N-][Si](C)(C)C.[Na+]
sodium bis(trimethylsilyl)amide
CC(C)(C)OC(=O)NCC(=CF)CO[Si](C)(C)C(C)(C)C
tert-butyl 2-((tert-butyldimethylsilyloxy)methyl)-3-fluoroallylcarbamate

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.WAITThe resulting deep orange solution was left
  2. 2
    workup.STIRRINGto stir at this temperature for 15 min
  3. 3
    workup.ADDITIONAfter complete addition
  4. 4
    workup.STIRRINGstirring
  5. 5
    기타The reaction was quenched by addition of water (5 mL)
  6. 6
    농축the reaction mixture was concentrated in vacuo
  7. 7
    기타The residue was partitioned between water (100 mL) and diethyl ether (100 mL)
  8. 8
    추출the aqueous layer was extracted with further diethyl ether (2×100 ml)
  9. 9
    건조The combined organics were dried over Na2SO4
  10. 10
    농축concentrated under reduced pressure
  11. 11
    기타The crude residue was purified over silica gel eluting with n-hexane

실험 절차

To a vigorously stirring suspension of fluoromethyl(triphenyl)-phosphonium tetrafluoroborate (18.9 g, 49.4 mmol) in dry THF (190 mL) at −20° C. under N2 was added sodium bis(trimethylsilyl)amide (1.0 M in THF; 49.4 mL, 49.4 mmol) slowly over 10 min. The resulting deep orange solution was left to stir at this temperature for 15 min. A solution of tert-butyl 3-(tert-butyldimethylsilyloxy)-2-oxopropylcarbamate (10.0 g, 33.0 mmol) in THF (10 mL) was then added slowly over 10 min. After complete addition, stirring was continued for a further 1 h during which time the reaction was allowed to warm slowly to room temperature. The reaction was quenched by addition of water (5 mL) and the reaction mixture was concentrated in vacuo. The residue was partitioned between water (100 mL) and diethyl ether (100 mL) and the aqueous layer was extracted with further diethyl ether (2×100 ml). The combined organics were dried over Na2SO4 and concentrated under reduced pressure. The crude residue was purified over silica gel eluting with n-hexane followed by 6% ethylacetate in n-hexane to give tert-butyl 2-((tert-butyldimethylsilyloxy)methyl)-3-fluoroallylcarbamate as a mixture of E/Z double-bond isomers (E/Z=1:1; 9.9 g; 94%). The isomers were not separated at this stage.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09302986B2uspto-grants-2016_04