2-[2-(2-{2-[2-(2-hydroxy-ethoxy)-benzylsulfanyl]-ethylsulfanyl}-ethylsulfanylmethyl)-phenoxy]-ethanol

Base Information

Chemical Name:2-[2-(2-{2-[2-(2-hydroxy-ethoxy)-benzylsulfanyl]-ethylsulfanyl}-ethylsulfanylmethyl)-phenoxy]-ethanol
CAS No.:506444-35-5
Molecular Formula:C₂₂H₃₀O₄S₃
Molecular Weight:454.676
Hs Code.:

Synonyms:2-[2-(2-{2-[2-(2-hydroxy-ethoxy)-benzylsulfanyl]-ethylsulfanyl}-ethylsulfanylmethyl)-phenoxy]-ethanol

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Chemical Property of 2-[2-(2-{2-[2-(2-hydroxy-ethoxy)-benzylsulfanyl]-ethylsulfanyl}-ethylsulfanylmethyl)-phenoxy]-ethanol

Chemical Property:

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Technology Process of 2-[2-(2-{2-[2-(2-hydroxy-ethoxy)-benzylsulfanyl]-ethylsulfanyl}-ethylsulfanylmethyl)-phenoxy]-ethanol

There total 4 articles about 2-[2-(2-{2-[2-(2-hydroxy-ethoxy)-benzylsulfanyl]-ethylsulfanyl}-ethylsulfanylmethyl)-phenoxy]-ethanol 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:

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

: 506444-35-5
2-[2-(2-{2-[2-(2-hydroxy-ethoxy)-benzylsulfanyl]-ethylsulfanyl}-ethylsulfanylmethyl)-phenoxy]-ethanol

Guidance literature:: Multi-step reaction with 4 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

4: 97 percent / LiAlH₄ / tetrahydrofuran / 0.08 h / 20 °C

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

Reference yield:

: 90-02-8
salicylaldehyde

: 506444-35-5
2-[2-(2-{2-[2-(2-hydroxy-ethoxy)-benzylsulfanyl]-ethylsulfanyl}-ethylsulfanylmethyl)-phenoxy]-ethanol

Guidance literature:: Multi-step reaction with 5 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

5: 97 percent / LiAlH₄ / tetrahydrofuran / 0.08 h / 20 °C

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

Reference yield:

: 111080-48-9
ethyl 2-[2-(hydroxymethyl)phenoxy]acetate

: 506444-35-5
2-[2-(2-{2-[2-(2-hydroxy-ethoxy)-benzylsulfanyl]-ethylsulfanyl}-ethylsulfanylmethyl)-phenoxy]-ethanol

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent / SOCl₂ / CH₂Cl₂ / 0.25 h / 0 °C

2: 100 percent / KOH / aq. ethanol; benzene / 1 h / 20 °C

3: 97 percent / LiAlH₄ / tetrahydrofuran / 0.08 h / 20 °C

With potassium hydroxide; lithium aluminium tetrahydride; thionyl chloride; In tetrahydrofuran; ethanol; dichloromethane; benzene;
DOI:10.1039/b205436a