[3-((1S,2R,3R,4R)-3-Hydroxymethyl-7-oxa-bicyclo[2.2.1]hept-2-ylmethyl)-phenyl]-acetic acid

Base Information

Chemical Name:[3-((1S,2R,3R,4R)-3-Hydroxymethyl-7-oxa-bicyclo[2.2.1]hept-2-ylmethyl)-phenyl]-acetic acid
CAS No.:1027988-54-0
Molecular Formula:C₁₆H₂₀O₄
Molecular Weight:276.332
Hs Code.:

Synonyms:[3-((1S,2R,3R,4R)-3-Hydroxymethyl-7-oxa-bicyclo[2.2.1]hept-2-ylmethyl)-phenyl]-acetic acid

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Chemical Property of [3-((1S,2R,3R,4R)-3-Hydroxymethyl-7-oxa-bicyclo[2.2.1]hept-2-ylmethyl)-phenyl]-acetic acid

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Technology Process of [3-((1S,2R,3R,4R)-3-Hydroxymethyl-7-oxa-bicyclo[2.2.1]hept-2-ylmethyl)-phenyl]-acetic acid

There total 7 articles about [3-((1S,2R,3R,4R)-3-Hydroxymethyl-7-oxa-bicyclo[2.2.1]hept-2-ylmethyl)-phenyl]-acetic acid 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:

: 127980-35-2
[3-((1S,2R,3R,4R)-3-Acetoxymethyl-7-oxa-bicyclo[2.2.1]hept-2-ylmethyl)-phenyl]-acetic acid

: 1027988-54-0
[3-((1S,2R,3R,4R)-3-Hydroxymethyl-7-oxa-bicyclo[2.2.1]hept-2-ylmethyl)-phenyl]-acetic acid

Guidance literature:: With sodium hydroxide; In tetrahydrofuran; at 25 ℃; for 0.5h;
DOI:10.1021/jm00113a030

Reference yield:

: 127980-30-7
<2-(3-bromophenyl)ethoxy>dimethyl(1,1,2-trimethylpropyl)silane

: 1027988-54-0
[3-((1S,2R,3R,4R)-3-Hydroxymethyl-7-oxa-bicyclo[2.2.1]hept-2-ylmethyl)-phenyl]-acetic acid

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) tBuLi / 1.) ether, -78 deg C, 2.) ether, THF, from -78 deg C to 0 deg C

2: H₂, AcOH / 20 percent Pd(OH)2-C / 760 Torr

3: DMAP, pyridine / 25 °C

4: CrO₃, H₂SO₄ / acetone / 0 - 25 °C

5: aq. NaOH / tetrahydrofuran / 25 °C

With pyridine; chromium(VI) oxide; dmap; sodium hydroxide; sulfuric acid; hydrogen; tert.-butyl lithium; acetic acid; palladium hydroxide - carbon; In tetrahydrofuran; acetone;
DOI:10.1021/jm00062a013

Reference yield:

: 127980-31-8
(3-{2-[Dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-ethyl}-phenyl)-((1S,2S,3R,4R)-3-hydroxymethyl-7-oxa-bicyclo[2.2.1]hept-2-yl)-methanol

: 1027988-54-0
[3-((1S,2R,3R,4R)-3-Hydroxymethyl-7-oxa-bicyclo[2.2.1]hept-2-ylmethyl)-phenyl]-acetic acid

Guidance literature:: Multi-step reaction with 4 steps

1: H₂, AcOH / 20 percent Pd(OH)2-C / 760 Torr

2: DMAP, pyridine / 25 °C

3: CrO₃, H₂SO₄ / acetone / 0 - 25 °C

4: aq. NaOH / tetrahydrofuran / 25 °C

With pyridine; chromium(VI) oxide; dmap; sodium hydroxide; sulfuric acid; hydrogen; acetic acid; palladium hydroxide - carbon; In tetrahydrofuran; acetone;
DOI:10.1021/jm00062a013