반응 #2021459

ord-86c8e3c66a1b49beb5ee60635881dccd

반응 방정식

COC(=O)[C@H]1[C@@H](OC(=O)c2ccccc2)C[C@@H]2CC[C@H]1N2C
(−)-cocaine
CN1[C@H]2CC[C@@H]1[C@@H](C(=O)O)[C@@H](O)C2
[1R-(exo,exo)]-3-hydroxy-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylic acid
수율 92.0%

반응물

시약

없음

용매

반응 조건

온도
112.5°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도(gentle reflux)
  2. 2
    온도After cooling to room temperature
  3. 3
    추출the mixture was thoroughly extracted with ether
  4. 4
    기타to remove the benzoic acid by-product
  5. 5
    기타The acidic aqueous layer was evaporated on a rotary evaporator under high vacuum
  6. 6
    workup.DISSOLUTIONthe residue was redissolved in water
  7. 7
    기타to afford a white solid that
  8. 8
    기타no further purification (92% yield)

실험 절차

Commercially available (−)-cocaine (Sigma Chemical Co.) was dissolved in 1.25 M HCl (1 g cocaine/12 ml). The mixture was allowed to stir for 16 hours at 110-115° C. (gentle reflux). After cooling to room temperature, the mixture was thoroughly extracted with ether to remove the benzoic acid by-product. The acidic aqueous layer was evaporated on a rotary evaporator under high vacuum and then the residue was redissolved in water and lyophilized to afford a white solid that required no further purification (92% yield).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06383490B1uspto-grants-2002_05