3-[1-(benzyl-tert-butylcarbamoyl)cyclopropyl]-3-oxopropionic acid ethyl ester

Base Information

Chemical Name:3-[1-(benzyl-tert-butylcarbamoyl)cyclopropyl]-3-oxopropionic acid ethyl ester
CAS No.:307964-76-7
Molecular Formula:C₂₀H₂₇NO₄
Molecular Weight:345.439
Hs Code.:

Synonyms:3-[1-(benzyl-tert-butylcarbamoyl)cyclopropyl]-3-oxopropionic acid ethyl ester

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Chemical Property of 3-[1-(benzyl-tert-butylcarbamoyl)cyclopropyl]-3-oxopropionic acid ethyl ester

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Technology Process of 3-[1-(benzyl-tert-butylcarbamoyl)cyclopropyl]-3-oxopropionic acid ethyl ester

There total 5 articles about 3-[1-(benzyl-tert-butylcarbamoyl)cyclopropyl]-3-oxopropionic acid ethyl ester 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:

: 1071-46-1
hydrogen ethyl malonate

: 1-(benzyl-tert-butylcarbamoyl)cyclopropanecarboxylic acid chloride

: 307964-76-7
3-[1-(benzyl-tert-butylcarbamoyl)cyclopropyl]-3-oxopropionic acid ethyl ester

Guidance literature:: hydrogen ethyl malonate; With isopropylmagnesium chloride; In dichloromethane; at 0 - 40 ℃;

1-(benzyl-tert-butylcarbamoyl)cyclopropanecarboxylic acid chloride; In dichloromethane; at 0 ℃; for 1h; Further stages.;
DOI:10.1021/jo0009144

Reference yield:

: 3697-66-3
1,1-cyclopropanedicarboxylic acid monoethyl ester

: 307964-76-7
3-[1-(benzyl-tert-butylcarbamoyl)cyclopropyl]-3-oxopropionic acid ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: (COCl)2; DMF / CH₂Cl₂ / 6 h

2.1: 18.1 g / CH₂Cl₂ / 12 h / 20 °C

3.1: 11.5 g / KOH / ethanol; H₂O / 24 h / 20 °C

4.1: (COCl)2; DMF / CH₂Cl₂ / 2 h / 20 °C

5.1: isopropylmagnesium chloride / CH₂Cl₂ / 0 - 40 °C

5.2: 1.2 g / CH₂Cl₂ / 1 h / 0 °C

With potassium hydroxide; oxalyl dichloride; isopropylmagnesium chloride; N,N-dimethyl-formamide; In ethanol; dichloromethane; water; 1.1: Substitution / 2.1: Condensation / 3.1: Hydrolysis / 4.1: Substitution / 5.1: Metallation / 5.2: Condensation;
DOI:10.1021/jo0009144

Reference yield:

: 3697-67-4
ethyl 1-chlorocarbonylcyclopropanecarboxylate

: 307964-76-7
3-[1-(benzyl-tert-butylcarbamoyl)cyclopropyl]-3-oxopropionic acid ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: 18.1 g / CH₂Cl₂ / 12 h / 20 °C

2.1: 11.5 g / KOH / ethanol; H₂O / 24 h / 20 °C

3.1: (COCl)2; DMF / CH₂Cl₂ / 2 h / 20 °C

4.1: isopropylmagnesium chloride / CH₂Cl₂ / 0 - 40 °C

4.2: 1.2 g / CH₂Cl₂ / 1 h / 0 °C

With potassium hydroxide; oxalyl dichloride; isopropylmagnesium chloride; N,N-dimethyl-formamide; In ethanol; dichloromethane; water; 1.1: Condensation / 2.1: Hydrolysis / 3.1: Substitution / 4.1: Metallation / 4.2: Condensation;
DOI:10.1021/jo0009144