- Process for preparation of β-(cyclopropylamino)acrylic acid esters, China, , ,
Cas no 96568-08-0 (2-Propenoic acid,3-(cyclopropylamino)-, ethyl ester)
96568-08-0 structure
Product Name:2-Propenoic acid,3-(cyclopropylamino)-, ethyl ester
CAS No:96568-08-0
MF:C8H13NO2
MW:155.194322347641
CID:800420
Update Time:2023-09-11
2-Propenoic acid,3-(cyclopropylamino)-, ethyl ester Chemical and Physical Properties
Names and Identifiers
-
- 2-Propenoic acid,3-(cyclopropylamino)-, ethyl ester
- ETHYL 3-(CYCLOPROPYLAMINO)ACRYLATE
- ethyl 3-(cyclopropylamino)prop-2-enoate
- Ethyl 3-(cyclopropylamino)-2-propenoate (ACI)
-
- Inchi: 1S/C8H13NO2/c1-2-11-8(10)5-6-9-7-3-4-7/h5-7,9H,2-4H2,1H3
- InChI Key: GCVNGUWEVLMYAJ-UHFFFAOYSA-N
- SMILES: O=C(C=CNC1CC1)OCC
2-Propenoic acid,3-(cyclopropylamino)-, ethyl ester Production Method
Production Method 1
Reaction Conditions
1.1 Solvents: Diisopropyl ether ; rt → reflux; 1.5 h, reflux; 4.5 h, reflux
Reference
Production Method 2
Reaction Conditions
Reference
- Synthesis of ethyl 3-cyclopropylaminoacrylateYang, Yongzheng; Gao, Yun; Li, Shaoxin, Zhongguo Yiyao Gongye Zazhi, 1992, 23(12),
Production Method 3
Reaction Conditions
1.1 Reagents: Sodium ethoxide Solvents: Toluene ; 6 h, 8 atm, 70 °C; 70 °C → 0 °C
1.2 Solvents: Toluene ; 35 min, 2 °C
1.2 Solvents: Toluene ; 35 min, 2 °C
Reference
- Process for preparation of 2-substituted-3-(N,N-disubstituted-amino)acrylates, World Intellectual Property Organization, , ,
Production Method 4
Reaction Conditions
1.1 Reagents: Carbon dioxide ; 1 - 2 atm, 60 °C
1.2 Reagents: Sodium ethoxide Solvents: Toluene ; 8 atm, rt → 70 °C; 6 h, 8 atm, 70 °C; 70 °C → 0 °C
1.3 Solvents: Toluene ; 35 min, 2 °C
1.2 Reagents: Sodium ethoxide Solvents: Toluene ; 8 atm, rt → 70 °C; 6 h, 8 atm, 70 °C; 70 °C → 0 °C
1.3 Solvents: Toluene ; 35 min, 2 °C
Reference
- Process for preparation of 2-substituted-3-(N,N-disubstituted-amino)acrylates, China, , ,
Production Method 5
Reaction Conditions
Reference
- Synthesis of 4H-1,4-benzothiazine 1-oxide and 1,1-dioxide. Analogs of quinoline antibacterial agentsCulbertson, Townley P., Journal of Heterocyclic Chemistry, 1991, 28(7), 1701-3
Production Method 6
Reaction Conditions
Reference
- Quinoline derivatives of β-lactams as antimicrobial compounds, World Intellectual Property Organization, , ,
2-Propenoic acid,3-(cyclopropylamino)-, ethyl ester Raw materials
- Ethyl formate
- Carbamic acid, cyclopropyl-
- ethyl propiolate
- cyclopropanamine
- sodium;ethyl 3-oxopropanoate
2-Propenoic acid,3-(cyclopropylamino)-, ethyl ester Preparation Products
2-Propenoic acid,3-(cyclopropylamino)-, ethyl ester Related Literature
-
Hanie Hashtroudi,Ian D. R. Mackinnon J. Mater. Chem. C, 2020,8, 13108-13126
-
Chao-Han Cheng,Wen-Zhen Wang,Shie-Ming Peng,I-Chia Chen Phys. Chem. Chem. Phys., 2017,19, 25471-25477
-
Matthew J. Gaunt,Jinquan Yu,Jonathan B. Spencer Chem. Commun., 2001, 1844-1845
-
Nan Fu,Naphaporn Chiewchan,Xiao Dong Chen Food Funct., 2020,11, 211-220
-
Dhirendra K. Chaudhary,Pramendra Kumar,Lokendra Kumar RSC Adv., 2016,6, 94731-94738
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