{4-[(1R,2S,3R)-1-tert-Butyl-3-(4-hydroxymethyl-benzyloxy)-2-(4-hydroxymethyl-benzyloxymethyl)-butoxymethyl]-phenyl}-methanol

Base Information

Chemical Name:{4-[(1R,2S,3R)-1-tert-Butyl-3-(4-hydroxymethyl-benzyloxy)-2-(4-hydroxymethyl-benzyloxymethyl)-butoxymethyl]-phenyl}-methanol
CAS No.:196880-46-3
Molecular Formula:C₃₃H₄₄O₆
Molecular Weight:536.709
Hs Code.:

Synonyms:{4-[(1R,2S,3R)-1-tert-Butyl-3-(4-hydroxymethyl-benzyloxy)-2-(4-hydroxymethyl-benzyloxymethyl)-butoxymethyl]-phenyl}-methanol

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Chemical Property of {4-[(1R,2S,3R)-1-tert-Butyl-3-(4-hydroxymethyl-benzyloxy)-2-(4-hydroxymethyl-benzyloxymethyl)-butoxymethyl]-phenyl}-methanol

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Technology Process of {4-[(1R,2S,3R)-1-tert-Butyl-3-(4-hydroxymethyl-benzyloxy)-2-(4-hydroxymethyl-benzyloxymethyl)-butoxymethyl]-phenyl}-methanol

There total 4 articles about {4-[(1R,2S,3R)-1-tert-Butyl-3-(4-hydroxymethyl-benzyloxy)-2-(4-hydroxymethyl-benzyloxymethyl)-butoxymethyl]-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: 83.0%

: dimethyl 4,4'-<<(2R,3S,4R)-3-<<4-(methoxycarbonyl)phenyl>methoxymethyl>-5,5-dimethylhexane-2,4-diyl>bis(oxymethylene)>bis(benzoate)

: 196880-46-3
{4-[(1R,2S,3R)-1-tert-Butyl-3-(4-hydroxymethyl-benzyloxy)-2-(4-hydroxymethyl-benzyloxymethyl)-butoxymethyl]-phenyl}-methanol

Guidance literature:: With lithium aluminium tetrahydride; In diethyl ether; for 5h; Heating;
DOI:10.1002/hlca.19940770702

Reference yield:

: 6232-88-8
4-bromomethylbenzoic Acid

: 196880-46-3
{4-[(1R,2S,3R)-1-tert-Butyl-3-(4-hydroxymethyl-benzyloxy)-2-(4-hydroxymethyl-benzyloxymethyl)-butoxymethyl]-phenyl}-methanol

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) NaH / 1.) THF, reflux, 7 d, 2.) ether, 1 h

2: 83 percent / LiAlH₄ / diethyl ether / 5 h / Heating

With lithium aluminium tetrahydride; sodium hydride; In diethyl ether;
DOI:10.1002/hlca.19940770702

Reference yield:

: 630-19-3
pivalaldehyde

: 196880-46-3
{4-[(1R,2S,3R)-1-tert-Butyl-3-(4-hydroxymethyl-benzyloxy)-2-(4-hydroxymethyl-benzyloxymethyl)-butoxymethyl]-phenyl}-methanol

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) (iPr)2NH, BuLi, 2.) AcCl, pyridine, 3.) LiAlH₄ / 1.) THF, hexane, -78 deg C, 4 h, 2.) RT, 9 h, 3.) ether, 0 deg C, then reflux, 4 h

2: 1.) NaH / 1.) THF, reflux, 7 d, 2.) ether, 1 h

3: 83 percent / LiAlH₄ / diethyl ether / 5 h / Heating

With pyridine; lithium aluminium tetrahydride; n-butyllithium; sodium hydride; diisopropylamine; acetyl chloride; In diethyl ether;
DOI:10.1002/hlca.19940770702