Carbamic acid, (1-oxo-2-butynyl)-, 1,1-dimethylethyl ester (9CI)

Base Information

Chemical Name:Carbamic acid, (1-oxo-2-butynyl)-, 1,1-dimethylethyl ester (9CI)
CAS No.:182495-32-5
Molecular Formula:C₉H₁₃NO₃
Molecular Weight:183.207
Hs Code.:
Mol file:182495-32-5.mol

Synonyms:Carbamic acid, (1-oxo-2-butynyl)-, 1,1-dimethylethyl ester (9CI)

Suppliers and Price of Carbamic acid, (1-oxo-2-butynyl)-, 1,1-dimethylethyl ester (9CI)

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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 Carbamic acid, (1-oxo-2-butynyl)-, 1,1-dimethylethyl ester (9CI)

Chemical Property:

PSA：0.00000
LogP:0.00000

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

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Technology Process of Carbamic acid, (1-oxo-2-butynyl)-, 1,1-dimethylethyl ester (9CI)

There total 2 articles about Carbamic acid, (1-oxo-2-butynyl)-, 1,1-dimethylethyl ester (9CI) 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: 26.0%

: 182495-17-6
((R)-1-Hydroxymethyl-but-2-ynyl)-carbamic acid tert-butyl ester

: 182495-32-5
(1-Oxo-but-2-ynyl)-carbamic acid tert-butyl ester

: 182495-27-8
(R)-2-tert-Butoxycarbonylamino-pent-3-ynoic acid

Guidance literature:: With jones reagent; In acetone; at 0 ℃; for 2h;
DOI:10.1016/0040-4020(96)00630-8

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 182495-32-5
(1-Oxo-but-2-ynyl)-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: aq. Na₂CO₃, NaHCO₃ / dioxane / 1.) 0 deg C, overnight, 2.) 25 deg C, 8 h

2: 24 percent / Jones reagent / acetone / 2 h / 0 °C

With jones reagent; sodium hydrogencarbonate; sodium carbonate; In 1,4-dioxane; acetone;
DOI:10.1016/0040-4020(96)00630-8