تفاعل #450994

ord-b4d4f82fcc0f4beaa9dcc69005f1e4de

معادلة التفاعل

Cc1ccccc1
toluene
COc1ccc2cc([C@H](C)C(=O)O)ccc2c1
(S)-2-(6-methoxy-2-naphthyl)propionic acid
COc1ccc2cc(C(C)C(=O)O)ccc2c1
racemic 2-(6-methoxy-2-naphthyl)propionic acid
[Na+].[OH-]
NaOH
COc1ccc2cc([C@H](C)C(=O)[O-])ccc2c1.[Na+]
sodium (S)-2-(6-methoxy-2-naphthyl)propionate
COc1ccc2cc(C(C)C(=O)O)ccc2c1
2-(6-methoxy-2-naphthyl)propionic acid
المردود 91.6%

المذيبات

ظروف التفاعل

درجة الحرارة
85°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىTwo clear liquid phases were obtained
  2. 2
    أخرىThe total amount of water collected during the strip
  3. 3
    أخرىthe amount of toluene removed
  4. 4
    درجة الحرارةcooled to 75° C. in 82 minutes
  5. 5
    workup.STIRRINGagitated at 75° C. for 60 minutes
  6. 6
    أخرىsettled well at the end of the 60-minute 75° C. ride
  7. 7
    غسيلThe centrifuge cake (sodium (S)-2-(6-methoxy-2-naphthyl)propionate monohydrate) was washed with 149.94 grams of hot (75° C.) toluene
  8. 8
    غسيلTotals of 483.77 and 127.61 grams of mother liquor and wash liquor
  9. 9
    أخرىwere recovered
  10. 10
    أخرىafter drying for 8 hours at 80°-90° C. and under full vacuum

الإجراء التجريبي

Using the apparatus of the above Comparative Example, a toluene solution of 2-(6-methoxy-2-naphthyl)propionic acid (580.68 grams, 18.11 wt % solids, 91.64% S-enantiomer) was prepared from a sample of high chiral purity (S)-2-(6-methoxy-2-naphthyl)propionic acid, and racemic 2-(6-methoxy-2-naphthyl)propionic acid. The solution was heated to 85° C. Totals of 27.59 grams of 49.22 wt % NaOH and 7.822 grams of water were added. Two clear liquid phases were obtained. Water was stripped to 94.0° C. in 285 minutes. The total amount of water collected during the strip was 21.36 grams and the amount of toluene removed was 1.83 grams. The batch was agitated at 93.6°-94.0° C. for 15 minutes and cooled to 75° C. in 82 minutes and agitated at 75° C. for 60 minutes. Solids in the slurry settled well at the end of the 60-minute 75° C. ride. The centrifuge cake (sodium (S)-2-(6-methoxy-2-naphthyl)propionate monohydrate) was washed with 149.94 grams of hot (75° C.) toluene. Totals of 483.77 and 127.61 grams of mother liquor and wash liquor were recovered, respectively. The wet centrifuge cake weighed 75.02 grams which after drying for 8 hours at 80°-90° C. and under full vacuum yielded 67.29 grams of anhydrous sodium (S)-2-(6-methoxy-2-naphthyl)propionate. Chiral purities for the product and the mother liquor were found by analysis to be 99.03% S-enantiomer and 80.28% S-enantiomer, respectively.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05874614uspto-grants-1999_02