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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329874Generated: October 31, 2026

Methyl 3-formylbenzoate → HCID 70351527, compound

https://huagongshe.com/reaction/329874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-formylbenzoateHCID 639145—
Reactant2-Butenoic acid, 3-amino-, ethyl ester, (2Z)-HCID 643756—
ReactantHCID 19871204HCID 19871204—
SolventIsopropanolHCID 3776—
ProductHCID 70351527HCID 7035152747.5%

Reaction Steps

A mixture of m-methoxycarbonylbenzaldehyde, 2-[4-(4,4'-dimethylbenzhydryl)-1-piperazinyl]ethyl acetoacetate and ethyl 3-aminocrotonate was worked up in isopropyl alcohol in the same manner as Example 1 to give 2-[4-(4,4'-dimethylbenzhydryl)-1-piperazinyl]ethyl ethy 4-(3-methoxycarbonylphenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate as a light yellow powder, m.p. 80°-83° C. (sintering). Yield 47.5%. IR(Nujol)cm-1 : 3330, 1720, 1690. NMR(CDCl3) δ: 1.17(3H,t,J=7,--CH2CH3), 2.25(6H,s, ##STR49## 2.31(6H,s, ##STR50## 3.83(3H,s,--COOCH3), 4.03(2H, q,J=7,--CH2CH3), 4.10(1H,s,>N--CH<), 4.10(2H,t,J=6, --COOCH2CH2 --), 5.00(1H,s,C(4) --H), 5.78(1H,broad s, NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04892875
Source datasetuspto-grants-1990_01
ORD IDord-27cd96607b9c416dabb5d2655fd50f8f
Source noteuspto-grants-1990_01