4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl 4-((phenoxycarbonyloxy)methyl)phenylcarbamate

Base Information

Chemical Name:4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl 4-((phenoxycarbonyloxy)methyl)phenylcarbamate
CAS No.:1349833-04-0
Molecular Formula:C₂₈H₃₀BNO₇
Molecular Weight:503.36
Hs Code.:

Synonyms:4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl 4-((phenoxycarbonyloxy)methyl)phenylcarbamate

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Chemical Property of 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl 4-((phenoxycarbonyloxy)methyl)phenylcarbamate

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Technology Process of 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl 4-((phenoxycarbonyloxy)methyl)phenylcarbamate

There total 5 articles about 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl 4-((phenoxycarbonyloxy)methyl)phenylcarbamate 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: 92.0%

: 1349833-53-9
4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl 4-(hydroxymethyl)phenylcarbamate

: 1885-14-9
phenyl chloroformate

: 1349833-04-0
4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl 4-((phenoxycarbonyloxy)methyl)phenylcarbamate

Guidance literature:: With dmap; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 25 ℃; for 12h; Inert atmosphere;
DOI:10.1021/jo2018763

Reference yield:

: 1349832-91-2
4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl 4-formylphenylcarbamate

: 1349833-04-0
4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl 4-((phenoxycarbonyloxy)methyl)phenylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium tetrahydroborate / methanol; dichloromethane / 0 - 25 °C / Inert atmosphere

2: dmap; N-ethyl-N,N-diisopropylamine / dichloromethane / 12 h / 25 °C / Inert atmosphere

With dmap; sodium tetrahydroborate; N-ethyl-N,N-diisopropylamine; In methanol; dichloromethane;
DOI:10.1021/jo2018763

Reference yield:

: 1349832-93-4
4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl 4-(dimethoxymethyl)phenylcarbamate

: 1349833-04-0
4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl 4-((phenoxycarbonyloxy)methyl)phenylcarbamate

Guidance literature:: Multi-step reaction with 3 steps

1: water-d2; [D₃]acetonitrile / 6 h / 25 °C / pH 10 / aq. buffer

2: sodium tetrahydroborate / methanol; dichloromethane / 0 - 25 °C / Inert atmosphere

3: dmap; N-ethyl-N,N-diisopropylamine / dichloromethane / 12 h / 25 °C / Inert atmosphere

With dmap; sodium tetrahydroborate; N-ethyl-N,N-diisopropylamine; In methanol; water-d2; dichloromethane; [D₃]acetonitrile;
DOI:10.1021/jo2018763