(R)-N-(1-phenyl-2-tert-butyldimethylsilylethoxy)-2-(3,4-methylenedioxyphenyl)acetamide

Base Information

Chemical Name:(R)-N-(1-phenyl-2-tert-butyldimethylsilylethoxy)-2-(3,4-methylenedioxyphenyl)acetamide
CAS No.:347378-39-6
Molecular Formula:C₂₃H₃₁NO₄Si
Molecular Weight:413.589
Hs Code.:

Synonyms:(R)-N-(1-phenyl-2-tert-butyldimethylsilylethoxy)-2-(3,4-methylenedioxyphenyl)acetamide

Suppliers and Price of (R)-N-(1-phenyl-2-tert-butyldimethylsilylethoxy)-2-(3,4-methylenedioxyphenyl)acetamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (R)-N-(1-phenyl-2-tert-butyldimethylsilylethoxy)-2-(3,4-methylenedioxyphenyl)acetamide

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Technology Process of (R)-N-(1-phenyl-2-tert-butyldimethylsilylethoxy)-2-(3,4-methylenedioxyphenyl)acetamide

There total 7 articles about (R)-N-(1-phenyl-2-tert-butyldimethylsilylethoxy)-2-(3,4-methylenedioxyphenyl)acetamide 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: 92.0%

: 6845-81-4
3,4-methylenedioxyphenylacetyl chloride

: 120417-13-2,120666-55-9
(1R)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-phenylethanamine

: 347378-39-6
(R)-N-(1-phenyl-2-tert-butyldimethylsilylethoxy)-2-(3,4-methylenedioxyphenyl)acetamide

Guidance literature:: With dmap; triethylamine; In dichloromethane; at 20 ℃; for 1h;
DOI:10.1021/jm001128u

Reference yield:

: 2861-28-1
1,3-benzodioxole-5-acetic acid

: 347378-39-6
(R)-N-(1-phenyl-2-tert-butyldimethylsilylethoxy)-2-(3,4-methylenedioxyphenyl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: SOCl₂ / CH₂Cl₂ / 3 h / Heating

2: 92 percent / 4-DMAP; Et₃N / CH₂Cl₂ / 1 h / 20 °C

With dmap; thionyl chloride; triethylamine; In dichloromethane;
DOI:10.1021/jm001128u

Reference yield:

: 326-59-0
benzo[1,3]dioxol-5-yl-acetic acid methyl ester

: 347378-39-6
(R)-N-(1-phenyl-2-tert-butyldimethylsilylethoxy)-2-(3,4-methylenedioxyphenyl)acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: 97 percent / 20percent aq. KOH / methanol / 3 h / Heating

2: SOCl₂ / CH₂Cl₂ / 3 h / Heating

3: 92 percent / 4-DMAP; Et₃N / CH₂Cl₂ / 1 h / 20 °C

With dmap; thionyl chloride; triethylamine; In methanol; dichloromethane;
DOI:10.1021/jm001128u