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Acetic Acid → HCID 14552383、化合物

HRID 1110774
ノート
印刷プレビュー

反応式

HRID 1110774 の反応式
[C:1]1([CH2:7][NH:8][C:9]2[CH2:18][CH2:17][C:12]3([O:16][CH2:15][CH2:14][O:13]3)[CH2:11][C:10]=2[C:19]([O:21][CH2:22][CH3:23])=[O:20])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C(O)(=O)C.C(O)C.C([BH3-])#N.[Na+]>C1COCC1.O>[C:1]1([CH2:7][NH:8][CH:9]2[CH2:18][CH2:17][C:12]3([O:16][CH2:15][CH2:14][O:13]3)[CH2:11][CH:10]2[C:19]([O:21][CH2:22][CH3:23])=[O:20])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 176Acetic AcidHCID 702EthanolHCID 5003444Sodium cyanoborohydrideHCID 14552382HCID 14552382、化合物

生成物 1

HCID 14552383HCID 14552383、化合物収率 99.9%

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 8028
Tetrahydrofuran
溶媒

実験手順

Ethyl 8-[(phenylmethyl)amino]-1,4-dioxaspiro-[4.5]-dec-7-ene-7-carboxylate (395.4 g, 1.3 mole) and acetic acid (75.0 ml, 1.3 mole) were added to ethanol (4 l). Sodium cyanoborohydride (82.0 g, 1.3 mole) was added in portions over 3 hours. The mixture was stirred overnight, then poured into water. The pH was adjusted to 10, and the product was extracted with methylene chloride, which was then dried with sodium sulfate and evaporated to give a yellow oil having small clear lumps in it. This was dissolved in THF and poured through 3 inches of basic alumina, which was then rinsed well with THF. The filtrate was evaporated to give 397.2 g (99.9%) of the title product as a yellow-green oil.

後処理

  1. extractionthe product was extracted with methylene chloride, which
  2. dry with materialwas then dried with sodium sulfate
  3. customevaporated
  4. customto give a yellow oil
  5. additionpoured through 3 inches of basic alumina, which
  6. washwas then rinsed well with THF
  7. customThe filtrate was evaporated

出典と根拠

ORDレコード
ord-bf921e5be4914ce7bd7e1d73297fb7d9
出典データセット
uspto-grants-1990_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04977160

反応ノート

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