2-{1-[(Tert-butoxy)carbonyl]-1,2,3,6-tetrahydropyridin-4-yl}acetic acid

Base Information

Chemical Name:2-{1-[(Tert-butoxy)carbonyl]-1,2,3,6-tetrahydropyridin-4-yl}acetic acid
CAS No.:817201-95-9
Molecular Formula:C₁₂H₁₉NO₄
Molecular Weight:241.287
Hs Code.:
European Community (EC) Number:886-816-5

Synonyms:817201-95-9;2-{1-[(tert-butoxy)carbonyl]-1,2,3,6-tetrahydropyridin-4-yl}acetic acid;2-[1-[(2-methylpropan-2-yl)oxycarbonyl]-3,6-dihydro-2H-pyridin-4-yl]acetic acid;SCHEMBL7149700;EN300-147709;Z1721257713

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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 2-{1-[(Tert-butoxy)carbonyl]-1,2,3,6-tetrahydropyridin-4-yl}acetic acid

Chemical Property:

XLogP3:0.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:241.13140809
Heavy Atom Count:17
Complexity:341

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)(C)OC(=O)N1CCC(=CC1)CC(=O)O

Technology Process of 2-{1-[(Tert-butoxy)carbonyl]-1,2,3,6-tetrahydropyridin-4-yl}acetic acid

There total 1 articles about 2-{1-[(Tert-butoxy)carbonyl]-1,2,3,6-tetrahydropyridin-4-yl}acetic acid 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:

: 84839-55-4
tert.butyl 1-tert.butyloxycarbonyl-Δ^4,α-piperidineacetate

: 193085-24-4
4-carboxymethylenepiperidine-1-carboxylic acid tert-butyl ester

: 817201-95-9
4-carboxymethyl-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester

Guidance literature:: tert.butyl 1-tert.butyloxycarbonyl-Δ^4,α-piperidineacetate; With ammonium chloride; sodium t-butanolate; In tert-butyl alcohol; at 20 - 100 ℃; for 0.5h;

With hydrogenchloride; In 1,3-dioxane; dichloromethane; at 0 - 20 ℃; for 1h;

With sodium hydroxide; t-butyl malonate; citric acid; more than 3 stages;