dimethyl [(RS)-1-(tert-butoxycarbonylamino)-3-(phenylsulfanyl)propyl]phosphonate

Base Information

Chemical Name:dimethyl [(RS)-1-(tert-butoxycarbonylamino)-3-(phenylsulfanyl)propyl]phosphonate
CAS No.:1367824-40-5
Molecular Formula:C₁₆H₂₆NO₅PS
Molecular Weight:375.426
Hs Code.:

Synonyms:dimethyl [(RS)-1-(tert-butoxycarbonylamino)-3-(phenylsulfanyl)propyl]phosphonate

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Chemical Property of dimethyl [(RS)-1-(tert-butoxycarbonylamino)-3-(phenylsulfanyl)propyl]phosphonate

Chemical Property:

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Technology Process of dimethyl [(RS)-1-(tert-butoxycarbonylamino)-3-(phenylsulfanyl)propyl]phosphonate

There total 5 articles about dimethyl [(RS)-1-(tert-butoxycarbonylamino)-3-(phenylsulfanyl)propyl]phosphonate 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: 55.0%

: 1367824-36-9
diphenyl [(RS)-1-(tert-butoxycarbonylamino)-3-(phenylsulfanyl)propyl]phosphonate

: 124-41-4
sodium methylate

: 1367824-40-5
dimethyl [(RS)-1-(tert-butoxycarbonylamino)-3-(phenylsulfanyl)propyl]phosphonate

Guidance literature:: With methanol; In 1,4-dioxane; at 20 ℃;

Reference yield:

: 27098-65-3
3-phenylsulfanyl-propionaldehyde

: 1367824-40-5
dimethyl [(RS)-1-(tert-butoxycarbonylamino)-3-(phenylsulfanyl)propyl]phosphonate

Guidance literature:: Multi-step reaction with 4 steps

1: acetic acid / 1 h / 80 °C

2: hydrogen bromide; acetic acid / water

3: triethylamine / dichloromethane / 0 - 20 °C

4: methanol / 1,4-dioxane / 20 °C

With methanol; hydrogen bromide; acetic acid; triethylamine; In 1,4-dioxane; dichloromethane; water;

Reference yield:

: 108-98-5
thiophenol

: 1367824-40-5
dimethyl [(RS)-1-(tert-butoxycarbonylamino)-3-(phenylsulfanyl)propyl]phosphonate

Guidance literature:: Multi-step reaction with 5 steps

1: triethylamine / dichloromethane / 0 - 20 °C

2: acetic acid / 1 h / 80 °C

3: hydrogen bromide; acetic acid / water

4: triethylamine / dichloromethane / 0 - 20 °C

5: methanol / 1,4-dioxane / 20 °C

With methanol; hydrogen bromide; acetic acid; triethylamine; In 1,4-dioxane; dichloromethane; water;