ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

HCID 54549910、化合物 → tert-butyl N-{6-azaspiro[3.4]octan-8-yl}carbamate

HRID 1445274
ノート
印刷プレビュー

反応式

HRID 1445274 の反応式
[C:1]([O:5][C:6]([NH:8][CH:9]1[C:13]2([CH2:16][CH2:15][CH2:14]2)[CH2:12][N:11]([C@@H](C2C=CC=CC=2)C)[CH2:10]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]>C(O)C.[Pd]>[C:1]([O:5][C:6]([NH:8][CH:9]1[C:13]2([CH2:14][CH2:15][CH2:16]2)[CH2:12][NH:11][CH2:10]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 54549910HCID 54549910、化合物

生成物 1

HCID 19354273tert-butyl N-{6-azaspiro[3.4]octan-8-yl}carbamate収率 102.6%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒

実験手順

To a solution of 4.1 g of 8-tert-butoxycarbonylamino-6-[1-(R)-phenylethyl]-6-azaspiro[3.4]octane in 60 ml of ethanol there was added 4.5 g of 5% palladium on charcoal (50% wet) and reduction was carried out under a hydrogen atmosphere (H2 pressure: 4 atm.) for 5 hrs. During the reduction, the reaction vessel was warmed by irradiation with a tungsten lamp. At 1 hr. from the beginning of the reduction, 2 g of the same catalyst was further added and the reduction continued for an additional 4 hours at the same condition to total 5 hours. The catalyst was removed by filtration and the solvent was removed under reduced pressure to yield 2.88 g of the titled compound.

後処理

  1. customfor 5 hrs
  2. temperatureDuring the reduction, the reaction vessel was warmed by irradiation with a tungsten lamp
  3. waitthe reduction continued for an additional 4 hours at the same condition to total 5 hours
  4. customThe catalyst was removed by filtration
  5. customthe solvent was removed under reduced pressure

出典と根拠

ORDレコード
ord-4aa35c46623640e281d35494f27fb570
出典データセット
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
USRE041149E1

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート