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Water → HCID 12945490、化合物

HRID 1702986
ノート
印刷プレビュー

反応式

HRID 1702986 の反応式
[CH3:1][N:2]1[CH2:7][CH2:6][CH:5]2[C:8](=[O:16])[C:9]3[CH:15]=[CH:14][CH:13]=[CH:12][C:10]=3[S:11][CH:4]2[CH2:3]1.[C:17]1([Li])[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.O>CCOCC>[CH3:1][N:2]1[CH2:7][CH2:6][CH:5]2[C:8]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)([OH:16])[C:9]3[CH:15]=[CH:14][CH:13]=[CH:12][C:10]=3[S:11][CH:4]2[CH2:3]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 12945489HCID 12945489、化合物HCID 178506676HCID 178506676、化合物

生成物 1

HCID 12945490HCID 12945490、化合物収率 38.4%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

40 g of 1,2,3,4,4a,10a-hexahydro-2-methyl-5H-[1]-benzothiopyrano[2,3-c]pyridin-5-one were dissolved in 2 liters of dry ether and the solution obtaining was cooled to 5° C. in an ice bath while 220 ml (2 moles) of phenyl lithium were added dropwise thereto over 30 minutes with the temperature held below 0° C. When the addition was complete, the ice bath was removed and the solution thus obtained was stirred at room temperature for 30 minutes. 3 liters of water were added dropwise thereto and the resultant suspension was stirred vigorously for 2 hours and then was filtered. The product was washed with water and ether and was dried to obtain 20.5 g of 2-methyl-5-phenyl-1,3,4,4a,5,10a-hexahydro-2H[1]benzothiopyrano[2,3-c]pyridin-5-ol (37% yield) melting at 176°-181° C.

後処理

  1. customthe solution obtaining
  2. additionwere added dropwise
  3. additionWhen the addition
  4. customthe ice bath was removed
  5. customthe solution thus obtained
  6. filtrationwas filtered
  7. washThe product was washed with water and ether
  8. customwas dried

出典と根拠

ORDレコード
ord-97d9bd2835b74c118cf0b5ad75b4b5e8
出典データセット
uspto-grants-1982_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04350697

反応ノート

読み込み中…

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