تفاعل #4354

ord-558929a71aa1437ba847c6cb70cee4f2

معادلة التفاعل

Cc1ccccc1S(=O)(=O)N[C@@H](CC(C)C)C(=O)CCC(C)C
resultant compound
Cc1ccccc1S(=O)(=O)N[C@@H](CC(C)C)C(=O)CCC(C)C
(4S)-2,8-Dimethyl-4-[(toluenesulfonyl)amino]-5-nonanone
C=[CH][Mg][Br]
vinyl magnesium bromide
C=CC(O)(CCC(C)C)[C@H](CC(C)C)NS(=O)(=O)c1ccccc1C
desired product
المردود 95.0%
C=CC(O)(CCC(C)C)[C@H](CC(C)C)NS(=O)(=O)c1ccccc1C
(4S)-2,8-Dimethyl-5-hydroxy-4-[(toluenesulfonyl)amino]-5-vinylnonane
المردود 95.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىquenched (8 ml H2O+2 ml brine)
  2. 2
    استخلاصextracted with ether (3×4 ml)
  3. 3
    غسيلThe combined ether phase was washed (4 ml brine)
  4. 4
    تجفيفdried (Na2SO4)
  5. 5
    ترشيحfiltered
  6. 6
    أخرىevaporated

الإجراء التجريبي

To a stirred 0° C. solution of the resultant compound of Example 5 (79 mg, 0.23 mmol) in dry THF (8 ml) was added vinyl magnesium bromide (1.5 ml of a 1.0M solution in THF) dropwise. The mixture was warmed (room temperature, 10 hours), quenched (8 ml H2O+2 ml brine), acidified with 0.1M H3PO4 (pH=7), and extracted with ether (3×4 ml). The combined ether phase was washed (4 ml brine), dried (Na2SO4), filtered, and evaporated to give 81 mg (95%) of the desired product as a 4:1 mixture of diastereomers.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04725583uspto-grants-1988_02