반응 #2304289

ord-c5855366ef4942c58f3f209297b6ba40

반응 방정식

CCC1(CO)COC1
3-ethyl-3-hydroxymethyloxetane
Cc1ccc(S(=O)(=O)Cl)cc1
p-toluenesulfonyl chloride
CCC1(COS(=O)(=O)c2ccc(C)cc2)COC1
3-[(tosyloxy)methyl]-3-ethyloxetane
수율 90.2%

용매

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwas added to it intermittently
  2. 2
    workup.STIRRINGKept at 0° C., this was stirred for 5 hours
  3. 3
    추출This was extracted with 500 ml of diethyl ether
  4. 4
    세척The diethyl ether layer was washed with 3% hydrochloric acid until its pH
  5. 5
    세척washed with saturated sodium carbonate solution and water in this order
  6. 6
    건조dried with anhydrous magnesium sulfate
  7. 7
    기타The solvent was evaporated away

실험 절차

116 g of 3-ethyl-3-hydroxymethyloxetane (Toa Gosei's trade name, OXT-101) was added to 500 ml of pyridine, and cooled to 0° C. with stirring. 190 g of p-toluenesulfonyl chloride divided into a few portions was added to it intermittently. Kept at 0° C., this was stirred for 5 hours, and then 1 L of ice-water was poured into the reaction mixture. This was extracted with 500 ml of diethyl ether. The diethyl ether layer was washed with 3% hydrochloric acid until its pH became acidic, and then washed with saturated sodium carbonate solution and water in this order, and thereafter dried with anhydrous magnesium sulfate. The solvent was evaporated away, and 243 g of 3-[(tosyloxy)methyl]-3-ethyloxetane was obtained.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07407691B2uspto-grants-2008_08