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Ammonia → 4-Allyl-4-amino-adamantan-1-ol

HRID 38447
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반응식

HRID 38447 반응식
[OH:1][C:2]12[CH2:11][CH:6]3[CH2:7][CH:8]([CH2:10][CH:4]([C:5]3=O)[CH2:3]1)[CH2:9]2.CO.[CH2:15](B1OC(C)(C)C(C)(C)O1)[CH:16]=[CH2:17].[NH3:27]>>[CH2:15]([C:5]1([NH2:27])[CH:6]2[CH2:11][C:2]3([OH:1])[CH2:9][CH:8]([CH2:10][CH:4]1[CH2:3]3)[CH2:7]2)[CH:16]=[CH2:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 222AmmoniaHCID 887MethanolHCID 64184IdramantoneHCID 27631714,4,5,5-Tetramethyl-2-(prop-2-en-1-yl)-1,3,2-dioxaborolane

생성물 1

HCID 583808924-Allyl-4-amino-adamantan-1-ol

실험 절차

5-Hydroxy-2-adamantanone (3.0 g, 18.1 mmol) was dissolved in a solution of ammonia in methanol (7N, 26 mL, 180 mmol, 10 eq.) and stirred for 15 min at room temperature. Then, 2-allyl-4,4,5,5-tetramethyl-1,3,2-dioxa-borolane (5.4 mL, 28.9 mmol, 1.6 eq.) was added dropwise. The reaction mixture was stirred for 16 h at room temperature before the volatiles were removed in vacuo. The residue was taken up in methanol twice and evaporated, then lyophilized from water to give 4-allyl-4-amino-adamantan-1-ol (3) as a mixture of diastereomers. Rt=1.05 min, 1.79 min (Method 2). Detected mass: 270.3 (M+H+).

후처리

  1. stirringThe reaction mixture was stirred for 16 h at room temperature before the volatiles
  2. customwere removed in vacuo
  3. customevaporated

출처 및 근거

ORD 기록
ord-14f8bc6d7c064fdfbbc208d3ebc4e80e
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08524737B2

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