(R)-1-(p-tolyl)allyl propylcarbamate

Base Information

Chemical Name:(R)-1-(p-tolyl)allyl propylcarbamate
CAS No.:1587704-75-3
Molecular Formula:C₁₄H₁₉NO₂
Molecular Weight:233.31
Hs Code.:

Synonyms:(R)-1-(p-tolyl)allyl propylcarbamate

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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)-1-(p-tolyl)allyl propylcarbamate

Chemical Property:

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Technology Process of (R)-1-(p-tolyl)allyl propylcarbamate

There total 2 articles about (R)-1-(p-tolyl)allyl propylcarbamate 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: 52.0%

: 107-10-8,42939-71-9
propylamine

: 952686-35-0
methyl p-methylphenylallyl carbonate

: 1587704-75-3
(R)-1-(p-tolyl)allyl propylcarbamate

: 1494998-77-4
N-propyl-1-(p-tolyl)prop-2-en-1-amine

: (S)-1-p-tolylallyl propylcarbamate

: (E)-3-p-tolylallyl propylcarbamate

Guidance literature:: With potassium phosphate; bis(1,5-cyclooctadiene)diiridium(I) dichloride; (3,5-dioxa-4-phospha-cyclohepta[2,1-a;3,4-a']dinaphthalen-4-yl)-bis-(1-phenyl-ethyl)-amine; In dimethyl sulfoxide; at 35 ℃; enantioselective reaction; Inert atmosphere; Schlenk technique;
DOI:10.1002/chem.201402388

Reference yield: 48.0%

: 107-10-8,42939-71-9
propylamine

: 124-38-9,18923-20-1
carbon dioxide

: 96000-21-4,2048-34-2
1-(3-chloro-1-propenyl)-4-methylbenzene

: 1587704-75-3
(R)-1-(p-tolyl)allyl propylcarbamate

: 1494998-77-4
N-propyl-1-(p-tolyl)prop-2-en-1-amine

Guidance literature:: With 1,4-diaza-bicyclo[2.2.2]octane; bis(1,5-cyclooctadiene)diiridium(I) dichloride; O,O'-(S)-(1,1'-dinaphthyl-2,2'-diyl)-N,N'-di-(S, S)-[phenylethylphosphoramidite]; In toluene; at 15 ℃; under 760.051 Torr; enantioselective reaction; Inert atmosphere; Schlenk technique;
DOI:10.1039/c4cc00413b