(S)-benzyl 6,8-Bis(benzyloxy)-1-oxo-3-pentylisochroman-7-carboxylate

Base Information

Chemical Name:(S)-benzyl 6,8-Bis(benzyloxy)-1-oxo-3-pentylisochroman-7-carboxylate
CAS No.:1347738-63-9
Molecular Formula:C₃₆H₃₆O₆
Molecular Weight:564.678
Hs Code.:

Synonyms:

Suppliers and Price of (S)-benzyl 6,8-Bis(benzyloxy)-1-oxo-3-pentylisochroman-7-carboxylate

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 (S)-benzyl 6,8-Bis(benzyloxy)-1-oxo-3-pentylisochroman-7-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (S)-benzyl 6,8-Bis(benzyloxy)-1-oxo-3-pentylisochroman-7-carboxylate

There total 8 articles about (S)-benzyl 6,8-Bis(benzyloxy)-1-oxo-3-pentylisochroman-7-carboxylate 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:

: C₃₇H₄₀O₇

: 1347738-63-9
(S)-benzyl 6,8-Bis(benzyloxy)-1-oxo-3-pentylisochroman-7-carboxylate

Guidance literature:: With Amberlyst 15; In dichloromethane; at 20 ℃;
DOI:10.1021/jo201988m

Reference yield:

: 6121-79-5
dimethyl 4-carboxy-3,5-dihydroxyhomophthalate

: 1347738-63-9
(S)-benzyl 6,8-Bis(benzyloxy)-1-oxo-3-pentylisochroman-7-carboxylate

Guidance literature:: Multi-step reaction with 7 steps

1.1: potassium carbonate / acetone / 18 h / 20 °C / Inert atmosphere; Reflux

2.1: lithium hydroxide monohydrate / tetrahydrofuran; water / 24 h / 0 - 20 °C

3.1: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dichloromethane / 3 h / 20 °C / Inert atmosphere

4.1: ethylmagnesium bromide / tetrahydrofuran / 2.75 h / 0 - 50 °C / Inert atmosphere

4.2: 20 °C / Inert atmosphere

5.1: dimethylsulfide borane complex; benzo[1,3,2]dioxaborole / tetrahydrofuran / -10 °C / Inert atmosphere

6.1: platinum(IV) oxide; hydrogen / ethyl acetate / 20 °C

7.1: Amberlyst 15^.(R). / dichloromethane / 20 °C

With dmap; platinum(IV) oxide; lithium hydroxide monohydrate; dimethylsulfide borane complex; ethylmagnesium bromide; hydrogen; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; benzo[1,3,2]dioxaborole; In tetrahydrofuran; dichloromethane; water; ethyl acetate; acetone;
DOI:10.1021/jo201988m

Reference yield:

: 100-39-0
benzyl bromide

: 1347738-63-9
(S)-benzyl 6,8-Bis(benzyloxy)-1-oxo-3-pentylisochroman-7-carboxylate

Guidance literature:: Multi-step reaction with 7 steps

1.1: potassium carbonate / acetone / 18 h / 20 °C / Inert atmosphere; Reflux

2.1: lithium hydroxide monohydrate / tetrahydrofuran; water / 24 h / 0 - 20 °C

3.1: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dichloromethane / 3 h / 20 °C / Inert atmosphere

4.1: ethylmagnesium bromide / tetrahydrofuran / 2.75 h / 0 - 50 °C / Inert atmosphere

4.2: 20 °C / Inert atmosphere

5.1: dimethylsulfide borane complex; benzo[1,3,2]dioxaborole / tetrahydrofuran / -10 °C / Inert atmosphere

6.1: platinum(IV) oxide; hydrogen / ethyl acetate / 20 °C

7.1: Amberlyst 15^.(R). / dichloromethane / 20 °C

With dmap; platinum(IV) oxide; lithium hydroxide monohydrate; dimethylsulfide borane complex; ethylmagnesium bromide; hydrogen; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; benzo[1,3,2]dioxaborole; In tetrahydrofuran; dichloromethane; water; ethyl acetate; acetone;
DOI:10.1021/jo201988m