Dicyclohexylamine → Boc-D-Met-OH (dicyclohexylammonium) salt

HRID 223601ノート

反応式

HRID 223601 の反応式
[CH:1]1([NH:7][CH:8]2[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[C:14]([O:18][C:19]([NH:21][C@@H:22]([C:27]([OH:29])=[O:28])[CH2:23][CH2:24][S:25][CH3:26])=[O:20])([CH3:17])([CH3:16])[CH3:15]>C(OCC)(=O)C>[CH:8]1([NH:7][CH:1]2[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]2)[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13]1.[C:14]([O:18][C:19]([NH:21][C@@H:22]([C:27]([OH:29])=[O:28])[CH2:23][CH2:24][S:25][CH3:26])=[O:20])([CH3:17])([CH3:15])[CH3:16]

参加物

4

実験手順

With stirring 146 ml. of dicyclohexylamine were slowly added in portions to the ethyl acetate solution. The dicyclohexylamine salt of N-t-butyloxycarbonyl D-methionine began to crystallize during the addition of the amine. After addition of the amine was completed, approximately 400 ml. of petroleum ether were added to the crystallization mixture which was cooled in an ice bath for approximately 2 hours to complete crystallization. The product was filtered and washed on the filter with cold petroleum ether and was dried at 40° C. in a vacuum oven. The dried product weighed 199.5 g. (63% yield) and melted at about 136°-138° C. [α]=-12.8° (methyl alcohol).

後処理

  1. customto crystallize during the addition of the amine
  2. additionAfter addition of the amine
  3. additionof petroleum ether were added to the crystallization mixture which
  4. temperaturewas cooled in an ice bath for approximately 2 hours
  5. customcrystallization
  6. filtrationThe product was filtered
  7. washwashed on the
  8. filtrationfilter with cold petroleum ether
  9. customwas dried at 40° C. in a vacuum oven
  10. custom(63% yield) and melted at about 136°-138° C. [α]=-12.8° (methyl alcohol)

出典と根拠

ORDレコード
ord-4ae94fa315dd49c8892ba84c8c1181d7
出典データセット
uspto-grants-1982_10
特許番号
US04355172

反応ノート

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