{4-[4''-(4-Hydroxymethyl-phenoxymethyl)-[1,1';3',1'']terphenyl-4-ylmethoxy]-phenyl}-methanol

Base Information

Chemical Name:{4-[4''-(4-Hydroxymethyl-phenoxymethyl)-[1,1';3',1'']terphenyl-4-ylmethoxy]-phenyl}-methanol
CAS No.:177798-45-7
Molecular Formula:C₃₄H₃₀O₄
Molecular Weight:502.61
Hs Code.:

Synonyms:{4-[4''-(4-Hydroxymethyl-phenoxymethyl)-[1,1';3',1'']terphenyl-4-ylmethoxy]-phenyl}-methanol

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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-[4''-(4-Hydroxymethyl-phenoxymethyl)-[1,1';3',1'']terphenyl-4-ylmethoxy]-phenyl}-methanol

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Technology Process of {4-[4''-(4-Hydroxymethyl-phenoxymethyl)-[1,1';3',1'']terphenyl-4-ylmethoxy]-phenyl}-methanol

There total 6 articles about {4-[4''-(4-Hydroxymethyl-phenoxymethyl)-[1,1';3',1'']terphenyl-4-ylmethoxy]-phenyl}-methanol 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: 95.0%

: 601513-58-0
C₃₄H₂₆O₄

: 177798-45-7
{4-[4''-(4-Hydroxymethyl-phenoxymethyl)-[1,1';3',1'']terphenyl-4-ylmethoxy]-phenyl}-methanol

Guidance literature:: With sodium tetrahydroborate; In methanol; at 20 ℃; for 6h;
DOI:10.1016/S0040-4020(03)00686-0

Reference yield: 90.0%

: 154488-10-5
C₃₆H₃₀O₆

: 177798-45-7
{4-[4''-(4-Hydroxymethyl-phenoxymethyl)-[1,1';3',1'']terphenyl-4-ylmethoxy]-phenyl}-methanol

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; for 6h; Heating;
DOI:10.1021/jo950957y

Reference yield:

: 19399-68-9
1,3-di(p-tolyl)benzene

: 177798-45-7
{4-[4''-(4-Hydroxymethyl-phenoxymethyl)-[1,1';3',1'']terphenyl-4-ylmethoxy]-phenyl}-methanol

Guidance literature:: Multi-step reaction with 3 steps

1: 80 percent / N-bromosuccinimide, benzoyl peroxide / CCl₄ / 40 h / Heating

2: 85 percent / K₂CO₃ / dimethylformamide / 48 h / 60 °C

3: 90 percent / LiAlH₄ / tetrahydrofuran / 6 h / Heating

With N-Bromosuccinimide; lithium aluminium tetrahydride; Perbenzoic acid; potassium carbonate; In tetrahydrofuran; tetrachloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo950957y