N-<(1-oxo-1,2,3,4-tetrahydro-2-naphthyl)acetyl>-4-(p-fluorobenzoyl)piperidine

Base Information

Chemical Name:N-<(1-oxo-1,2,3,4-tetrahydro-2-naphthyl)acetyl>-4-(p-fluorobenzoyl)piperidine
CAS No.:157131-44-7
Molecular Formula:C₂₄H₂₄FNO₃
Molecular Weight:393.458
Hs Code.:

Synonyms:N-<(1-oxo-1,2,3,4-tetrahydro-2-naphthyl)acetyl>-4-(p-fluorobenzoyl)piperidine

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-<(1-oxo-1,2,3,4-tetrahydro-2-naphthyl)acetyl>-4-(p-fluorobenzoyl)piperidine

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Technology Process of N-<(1-oxo-1,2,3,4-tetrahydro-2-naphthyl)acetyl>-4-(p-fluorobenzoyl)piperidine

There total 5 articles about N-<(1-oxo-1,2,3,4-tetrahydro-2-naphthyl)acetyl>-4-(p-fluorobenzoyl)piperidine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 85.0%

: 56346-57-7
(4-fluorophenyl)-piperidin-4-ylmethanone

: 111735-12-7
1-oxo-1,2,3,4-tetrahydro-2-naphthaleneacetic acid chloride

: 157131-44-7
N-<(1-oxo-1,2,3,4-tetrahydro-2-naphthyl)acetyl>-4-(p-fluorobenzoyl)piperidine

Guidance literature:: In toluene; a) RT, 1 h, b) reflux, 24 h;

Reference yield: 81.0%

: 56346-57-7
(4-fluorophenyl)-piperidin-4-ylmethanone

: 6742-31-0
1,2,3,4-tetrahydro-1-oxo-2-naphthaleneacetic acid

: 157131-44-7
N-<(1-oxo-1,2,3,4-tetrahydro-2-naphthyl)acetyl>-4-(p-fluorobenzoyl)piperidine

Guidance literature:: With benzotriazol-1-ol; dicyclohexyl-carbodiimide; at 0 - 20 ℃; for 17h;

Reference yield:

: 41059-51-2
1-oxo-1,2,3,4-tetrahydro-2-naphthaleneacetic acid ethyl ester

: 157131-44-7
N-<(1-oxo-1,2,3,4-tetrahydro-2-naphthyl)acetyl>-4-(p-fluorobenzoyl)piperidine

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / conc. aq. HCl

2: 81 percent / N-hydroxybenzotriazole, N,N-dicyclohexylcarbodiimide / 17 h / 0 - 20 °C

With hydrogenchloride; benzotriazol-1-ol; dicyclohexyl-carbodiimide;