phenylmethyl 4-quinolylmethyl decanedioate

Base Information

Chemical Name:phenylmethyl 4-quinolylmethyl decanedioate
CAS No.:251922-72-2
Molecular Formula:C₂₇H₃₁NO₄
Molecular Weight:433.547
Hs Code.:

Synonyms:phenylmethyl 4-quinolylmethyl decanedioate

Suppliers and Price of phenylmethyl 4-quinolylmethyl decanedioate

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of phenylmethyl 4-quinolylmethyl decanedioate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of phenylmethyl 4-quinolylmethyl decanedioate

There total 3 articles about phenylmethyl 4-quinolylmethyl decanedioate 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%

: 6281-32-9
4-quinolylmethanol

: 111-19-3
sebacoyl chloride

: 100-51-6,185532-71-2
benzyl alcohol

: 251922-72-2
phenylmethyl 4-quinolylmethyl decanedioate

Guidance literature:: 4-quinolylmethanol; sebacoyl chloride; With dmap; triethylamine; In dichloromethane; at 20 ℃; for 4h;

benzyl alcohol; In dichloromethane; at 20 ℃; for 24h;
DOI:10.1016/S0040-4020(99)01108-4

Reference yield:

: 4363-93-3
quinoline-4-carboxaldehyde

: 251922-72-2
phenylmethyl 4-quinolylmethyl decanedioate

Guidance literature:: Multi-step reaction with 2 steps

1.1: 99 percent / NaBH₄ / ethanol / 1 h / 20 °C

2.1: Et₃N; DMAP / CH₂Cl₂ / 4 h / 20 °C

2.2: 85 percent / CH₂Cl₂ / 24 h / 20 °C

With dmap; sodium tetrahydroborate; triethylamine; In ethanol; dichloromethane; 1.1: Reduction / 2.1: Acylation / 2.2: Acylation;
DOI:10.1016/S0040-4020(99)01108-4