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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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tert-Butyl 7-benzyl-1-oxa-4,7-diazaspiro[5.4]decane-4-carboxylate → tert-Butyl 1-oxa-4,7-diazaspiro[5.4]decane-4-carboxylate

HRID 8576
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인쇄 미리보기

반응식

HRID 8576 반응식
C([N:8]1[CH2:24][CH2:23][CH2:22][C:9]21[O:14][CH2:13][CH2:12][N:11]([C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16])[CH2:10]2)C1C=CC=CC=1>CO.[Pd]>[O:14]1[C:9]2([CH2:22][CH2:23][CH2:24][NH:8]2)[CH2:10][N:11]([C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16])[CH2:12][CH2:13]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 21983523tert-Butyl 7-benzyl-1-oxa-4,7-diazaspiro[5.4]decane-4-carboxylate

생성물 1

HCID 21983552tert-Butyl 1-oxa-4,7-diazaspiro[5.4]decane-4-carboxylate

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

13.7 g (41 mmol) of tert-butyl 7-benzyl-1-oxa-4,7-diazaspiro[5.4]decane-4-carboxylate are dissolved in 300 ml of methanol, 3.0 g of 10% palladium on activated carbon are added, and hydrogenation is carried out at 100° C. and 100 bar. The catalyst is filtered off with suction, the filtrate is concentrated, and residue is distilled under high vacuum. 7.6 g (75% of theory) of the product are obtained.

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후처리

  1. customis carried out at 100° C.
  2. filtrationThe catalyst is filtered off with suction
  3. concentrationthe filtrate is concentrated
  4. distillationresidue is distilled under high vacuum
  5. custom7.6 g (75% of theory) of the product are obtained

출처 및 근거

ORD 기록
ord-203ff97b1a6344499f1a81b6bc4020cf
출처 데이터셋
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07091198B1

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