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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713853Generated: October 30, 2026

Ethyl 2-(3-(4-aminophenyl)cyclohexyl)acetate → Ethyl [(3S)-3-(4-aminophenyl)cyclopentylidene]acetate

https://huagongshe.com/reaction/1713853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-(3-(4-aminophenyl)cyclohexyl)acetateHCID 59464273—
Reactantethyl ((3S)-3-{4-[(diphenylmethylene)amino]phenyl}cyclopentylidene)acetateHCID 86619817—
ProductEthyl [(3S)-3-(4-aminophenyl)cyclopentylidene]acetateHCID 86619816—

Reaction Steps

Following the procedure described for ethyl [3-(4-aminophenyl)cyclohexyl]acetate (Intermediate 89(iv)), replacing ethyl (3-{4-[(diphenylmethylene)amino]phenyl}cyclohexyl)acetate with ethyl ((3S)-3-{4-[(diphenylmethylene)amino]phenyl}cyclopentylidene)acetate the title compound was obtained; 1H NMR δ 1.17-1.22 (3H, m), 1.57-1.68 (1H, m), 2.27-2.48 (2H, m), 2.53 (OH, s), 2.56-2.68 (1H, m), 2.74-2.76 (1H, m), 2.93-3.00 (1H, m), 3.15-3.24 (0.5H, m), 3.69-3.71 (0.5H, m), 4.01-4.12 (2H, m), 4.79-4.83 (2H, m), 5.49-5.53 (1H, m), 5.78-5.82 (1H, m), 6.47-6.52 (2H, m), 6.80-6.93 (2H, m); MS m/e M+MeCN 287.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795283B2
Source datasetuspto-grants-2010_09
ORD IDord-250650d388a948f889d08ecffaec5537
Source noteuspto-grants-2010_09