4--(3R)-piperidinyloxy>benzaldehyde

Base Information

Chemical Name:4--(3R)-piperidinyloxy>benzaldehyde
CAS No.:224954-08-9
Molecular Formula:C₃₃H₃₉NO₄
Molecular Weight:513.677
Hs Code.:

4-<N-<(3R/S)-5-benzyloxy-2,3-dihydro-2,2,4,6,7-pentamethyl-1-benzofuran-3-ylmethyl>-(3R)-piperidinyloxy>benzaldehyde

Synonyms:4--(3R)-piperidinyloxy>benzaldehyde

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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 4--(3R)-piperidinyloxy>benzaldehyde

Chemical Property:

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Technology Process of 4--(3R)-piperidinyloxy>benzaldehyde

There total 4 articles about 4--(3R)-piperidinyloxy>benzaldehyde 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: 35.0%

: 123-08-0,65581-83-1
4-hydroxy-benzaldehyde

: 199108-89-9
N-<(3R/S)-5-benzyloxy-2,3-dihydro-2,2,4,6,7-pentamethyl-1-benzofuran-3-ylmethyl>-(3R)-chloropiperidine

: 199109-07-4
4--(2S)-pyrrolidin-2-ylmethoxy>benzaldehyde

: 224954-08-9
4--(3R)-piperidinyloxy>benzaldehyde

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 80 ℃; for 12h;
DOI:10.1021/jm980549x

Reference yield:

: 183142-41-8
5-benzyloxy-2,2,4,6,7-pentamethyl-1-benzofuran-3-carbinol

: 224954-08-9
4--(3R)-piperidinyloxy>benzaldehyde

Guidance literature:: Multi-step reaction with 4 steps

1: 99 percent / Et₃N / CH₂Cl₂ / 3 h / 25 °C

2: 73 percent / 12 h / 120 °C

3: 91 percent / SOCl₂ / benzene / 1 h / Ambient temperature

4: 34 percent / K₂CO₃ / dimethylformamide / 12 h / 80 °C

With thionyl chloride; potassium carbonate; triethylamine; In dichloromethane; N,N-dimethyl-formamide; benzene;
DOI:10.1021/jm980549x

Reference yield:

: 187341-65-7
5-benzyloxy-2,2,4,6,7-pentamethyl-1-benzofuran-3-ylmethyl methanesulfonate

: 224954-08-9
4--(3R)-piperidinyloxy>benzaldehyde

Guidance literature:: Multi-step reaction with 3 steps

1: 73 percent / 12 h / 120 °C

2: 91 percent / SOCl₂ / benzene / 1 h / Ambient temperature

3: 34 percent / K₂CO₃ / dimethylformamide / 12 h / 80 °C

With thionyl chloride; potassium carbonate; In N,N-dimethyl-formamide; benzene;
DOI:10.1021/jm980549x