반응 #55052

ord-85a410fa440942bfa0c0283cc6c9bcf7

반응 방정식

CCOCC.FB(F)F
boron trifluoride etherate
C=C(C)C
isobutylene
O=P(O)(O)O
phosphoric acid
O=C([O-])O.[Na+]
NaHCO3
ClCCl
CH2Cl2
CC(C)=O.O=C=O
dry ice acetone
ClCCl
CH2Cl2
C[C@@H](COC(C)(C)C)C(=O)OC(C)(C)C
desired product
C[C@@H](COC(C)(C)C)C(=O)OC(C)(C)C
(S)-(+)tert. Butyl 3-tert. butoxy-2-methylpropionate

용매

반응 조건

온도
-72°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONTo the resulting mixture was added
  2. 2
    workup.STIRRINGThe resulting mixture was stirred at -72° C. for 2 hours and at 0-5° C. (ice bath) for 20 hours
  3. 3
    workup.ADDITIONthen treated with 300 g
  4. 4
    기타The CH2Cl2 layer was removed
  5. 5
    추출the aqueous layer was extracted twice with CH 2 Cl2
  6. 6
    세척The combined organic extracts were washed twice with brine
  7. 7
    건조then dried (MgSO4)
  8. 8
    여과filtered
  9. 9
    농축concentrated in vacuo
  10. 10
    기타giving 23.3 g
  11. 11
    기타This material was chromatographed on 200 g
  12. 12
    세척Elution with 19:1 parts by volume and 9:1 parts by volume hexane-ether

실험 절차

A solution of 8.7 g. of S-(+)-β-hydroxyisobutyric acid in 140 ml. of CH2Cl2 was stirred and cooled to -72° C. (dry ice-acetone bath) whereupon 70 ml. of liquid isobutylene was added rapidly. To the resulting mixture was added with stirring at -72° C., a solution of 1.6 ml. of phosphoric acid (prepared by dissolving 5 g. of phosphorus pentoxide in 11 ml. of 85% by weight phosphoric acid) in 10 ml. of CH2Cl2, dropwise followed by 3.5 ml. of boron trifluoride etherate also dropwise. The resulting mixture was stirred at -72° C. for 2 hours and at 0-5° C. (ice bath) for 20 hours then treated with 300 g. of ice-water followed by a solution of 19 g. of NaHCO3 in 200 ml. of water. The CH2Cl2 layer was removed and the aqueous layer was extracted twice with CH 2 Cl2. The combined organic extracts were washed twice with brine then dried (MgSO4), filtered and concentrated in vacuo giving 23.3 g. of crude product as a yellow oil. This material was chromatographed on 200 g. of silica gel. Elution with 19:1 parts by volume and 9:1 parts by volume hexane-ether gave the desired product which was distilled yielding 12.7 g. (79%) of the ether ester (S)-(+)-tert. butyl 3-tert. butoxy-2-methylpropionate as a colorless liquid, b.p. 99° C. (22 mm Hg.); [α]25D+ 19.52° (c 4.25, CH3OH).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04151205uspto-grants-1979_04