(2-{2-[2-(2-ethoxycarbonylmethoxy-benzylsulfanyl)-ethylsulfanyl]-ethylsulfanylmethyl}-phenoxy)-acetic acid ethyl ester

Base Information

Chemical Name:(2-{2-[2-(2-ethoxycarbonylmethoxy-benzylsulfanyl)-ethylsulfanyl]-ethylsulfanylmethyl}-phenoxy)-acetic acid ethyl ester
CAS No.:506444-33-3
Molecular Formula:C₂₆H₃₄O₆S₃
Molecular Weight:538.75
Hs Code.:

Synonyms:(2-{2-[2-(2-ethoxycarbonylmethoxy-benzylsulfanyl)-ethylsulfanyl]-ethylsulfanylmethyl}-phenoxy)-acetic acid ethyl ester

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Chemical Property of (2-{2-[2-(2-ethoxycarbonylmethoxy-benzylsulfanyl)-ethylsulfanyl]-ethylsulfanylmethyl}-phenoxy)-acetic acid ethyl ester

Chemical Property:

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Technology Process of (2-{2-[2-(2-ethoxycarbonylmethoxy-benzylsulfanyl)-ethylsulfanyl]-ethylsulfanylmethyl}-phenoxy)-acetic acid ethyl ester

There total 4 articles about (2-{2-[2-(2-ethoxycarbonylmethoxy-benzylsulfanyl)-ethylsulfanyl]-ethylsulfanylmethyl}-phenoxy)-acetic acid ethyl ester 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: 100.0%

: 3570-55-6
3-thiapentan-1,5-dithiol

: 111080-49-0
o-(ethoxycarbonylmethoxy)benzyl chloride

: 506444-33-3
(2-{2-[2-(2-ethoxycarbonylmethoxy-benzylsulfanyl)-ethylsulfanyl]-ethylsulfanylmethyl}-phenoxy)-acetic acid ethyl ester

Guidance literature:: With potassium hydroxide; In ethanol; benzene; at 20 ℃; for 1h;
DOI:10.1039/b205436a

Reference yield:

: 41873-61-4
ethyl (2-formylphenoxy)acetate

: 506444-33-3
(2-{2-[2-(2-ethoxycarbonylmethoxy-benzylsulfanyl)-ethylsulfanyl]-ethylsulfanylmethyl}-phenoxy)-acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / NaBH₄ / methanol / 0.25 h / -5 - 0 °C

2: 92 percent / SOCl₂ / CH₂Cl₂ / 0.25 h / 0 °C

3: 100 percent / KOH / aq. ethanol; benzene / 1 h / 20 °C

With potassium hydroxide; sodium tetrahydroborate; thionyl chloride; In methanol; ethanol; dichloromethane; benzene;
DOI:10.1039/b205436a

Reference yield:

: 90-02-8
salicylaldehyde

: 506444-33-3
(2-{2-[2-(2-ethoxycarbonylmethoxy-benzylsulfanyl)-ethylsulfanyl]-ethylsulfanylmethyl}-phenoxy)-acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 88 percent / K₂CO₃ / acetone / Heating

2: 95 percent / NaBH₄ / methanol / 0.25 h / -5 - 0 °C

3: 92 percent / SOCl₂ / CH₂Cl₂ / 0.25 h / 0 °C

4: 100 percent / KOH / aq. ethanol; benzene / 1 h / 20 °C

With potassium hydroxide; sodium tetrahydroborate; thionyl chloride; potassium carbonate; In methanol; ethanol; dichloromethane; acetone; benzene;
DOI:10.1039/b205436a