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Ethyl 2-formylbutanoate → HCID 51029584, 화합물

HRID 2171741
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HRID 2171741 반응식
[CH3:1][C:2]1([CH3:20])[CH2:11][CH2:10][CH2:9][C:8]2[CH:7]=[C:6]([O:12][CH2:13][CH:14]3[O:18][C:17]([NH2:19])=[N:16][CH2:15]3)[CH:5]=[CH:4][C:3]1=2.C([O:23][C:24](=O)[CH:25]([CH:28]=O)[CH2:26][CH3:27])C>C(O)C>[CH3:1][C:2]1([CH3:20])[CH2:11][CH2:10][CH2:9][C:8]2[CH:7]=[C:6]([O:12][CH2:13][C@H:14]3[O:18][C:17]4=[N:19][C:24](=[O:23])[C:25]([CH2:26][CH3:27])=[CH:28][N:16]4[CH2:15]3)[CH:5]=[CH:4][C:3]1=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 289299Ethyl 2-formylbutanoateHCID 67053798HCID 67053798, 화합물

생성물 1

HCID 51029584HCID 51029584, 화합물수율 23.3%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of 5-(5,5-dimethyl-5,6,7,8-tetrahydro-naphthalen-2-yloxymethyl)-4,5-dihydro-oxazol-2-ylamine (0.5 g, 1.82 mmol) in ethanol (16 mL) was added 2-formyl-butyric acid ethyl ester (0.39 g, 2.7 mmol). The reaction mixture was stirred at room temperature for one hour, and then heated at reflux for 24 hours. It was then concentrated and loaded on a silica gel column. Chromatography with (1-5%) 2-propanol/methylene chloride gave 0.15 g the title product. [α]D25=−26.8 (c=0.74, CHCl3).

후처리

  1. temperatureheated
  2. temperatureat reflux for 24 hours
  3. concentrationIt was then concentrated

출처 및 근거

ORD 기록
ord-784585f0491a4810bf794b5f4a77cf0b
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09051331B2

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