(R)-2-[3,4-bis(benzyloxy)benzyl]-2,N-dimethyl-N-[(R)-1-(naphthalen-1-yl)ethyl]-2H-azirin-3-amine

Base Information

Chemical Name:(R)-2-[3,4-bis(benzyloxy)benzyl]-2,N-dimethyl-N-[(R)-1-(naphthalen-1-yl)ethyl]-2H-azirin-3-amine
CAS No.:501085-80-9
Molecular Formula:C₃₇H₃₆N₂O₂
Molecular Weight:540.705
Hs Code.:

Synonyms:(R)-2-[3,4-bis(benzyloxy)benzyl]-2,N-dimethyl-N-[(R)-1-(naphthalen-1-yl)ethyl]-2H-azirin-3-amine

Suppliers and Price of (R)-2-[3,4-bis(benzyloxy)benzyl]-2,N-dimethyl-N-[(R)-1-(naphthalen-1-yl)ethyl]-2H-azirin-3-amine

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (R)-2-[3,4-bis(benzyloxy)benzyl]-2,N-dimethyl-N-[(R)-1-(naphthalen-1-yl)ethyl]-2H-azirin-3-amine

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (R)-2-[3,4-bis(benzyloxy)benzyl]-2,N-dimethyl-N-[(R)-1-(naphthalen-1-yl)ethyl]-2H-azirin-3-amine

There total 5 articles about (R)-2-[3,4-bis(benzyloxy)benzyl]-2,N-dimethyl-N-[(R)-1-(naphthalen-1-yl)ethyl]-2H-azirin-3-amine 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:

: 501085-78-5
(RS)-2-[3,4-bis(benzyloxy)benzyl]-N-methyl-N-[(R)-1-(naphthalen-1-yl)ethyl]propanethioamide

: 501085-79-6
(S)-2-[3,4-bis(benzyloxy)benzyl]-2,N-dimethyl-N-[(R)-1-(naphthalen-1-yl)ethyl]-2H-azirin-3-amine

: 501085-80-9
(R)-2-[3,4-bis(benzyloxy)benzyl]-2,N-dimethyl-N-[(R)-1-(naphthalen-1-yl)ethyl]-2H-azirin-3-amine

Guidance literature:: (RS)-2-[3,4-bis(benzyloxy)benzyl]-N-methyl-N-[(R)-1-(naphthalen-1-yl)ethyl]propanethioamide; With N,N-dimethyl-formamide; In dichloromethane; toluene; at 0 ℃; for 0.25h;

With 1,4-diaza-bicyclo[2.2.2]octane; In tetrahydrofuran; at 0 ℃; for 0.333333h;

With sodium azide; In tetrahydrofuran; at 20 ℃; for 26h;
DOI:10.1002/1522-2675(200210)85:10<3422::AID-HLCA3422>3.0.CO;2-N

Reference yield:

: 5447-02-9
3,4-dibenzyloxybenzaldehyde

: 501085-80-9
(R)-2-[3,4-bis(benzyloxy)benzyl]-2,N-dimethyl-N-[(R)-1-(naphthalen-1-yl)ethyl]-2H-azirin-3-amine

Guidance literature:: Multi-step reaction with 5 steps

1.1: NaBH₄ / tetrahydrofuran / 4.5 h / 20 °C

2.1: 100 percent / PBr₃ / CH₂Cl₂ / 1.5 h / 0 - 20 °C

3.1: lithium diisopropylamide / tetrahydrofuran; heptane; ethylbenzene / 0.5 h / 0 °C

3.2: 88 percent / tetrahydrofuran; heptane; ethylbenzene / 2.58 h / 0 - 5 °C

4.1: 85 percent / Lawesson reagent / toluene / 5 h / 130 °C

5.1: DMF; COCl₂ / CH₂Cl₂; toluene / 0.25 h / 0 °C

5.2: 1,4-diazabicyclo[2.2.2]octane / tetrahydrofuran / 0.33 h / 0 °C

5.3: NaN₃ / tetrahydrofuran / 26 h / 20 °C

With Lawessons reagent; sodium tetrahydroborate; phosphorus tribromide; N,N-dimethyl-formamide; lithium diisopropyl amide; In tetrahydrofuran; n-heptane; dichloromethane; ethylbenzene; toluene;
DOI:10.1002/1522-2675(200210)85:10<3422::AID-HLCA3422>3.0.CO;2-N

Reference yield:

: 1699-58-7
3,4-bis(benzyloxy)benzyl alcohol

: 501085-80-9
(R)-2-[3,4-bis(benzyloxy)benzyl]-2,N-dimethyl-N-[(R)-1-(naphthalen-1-yl)ethyl]-2H-azirin-3-amine

Guidance literature:: Multi-step reaction with 4 steps

1.1: 100 percent / PBr₃ / CH₂Cl₂ / 1.5 h / 0 - 20 °C

2.1: lithium diisopropylamide / tetrahydrofuran; heptane; ethylbenzene / 0.5 h / 0 °C

2.2: 88 percent / tetrahydrofuran; heptane; ethylbenzene / 2.58 h / 0 - 5 °C

3.1: 85 percent / Lawesson reagent / toluene / 5 h / 130 °C

4.1: DMF; COCl₂ / CH₂Cl₂; toluene / 0.25 h / 0 °C

4.2: 1,4-diazabicyclo[2.2.2]octane / tetrahydrofuran / 0.33 h / 0 °C

4.3: NaN₃ / tetrahydrofuran / 26 h / 20 °C

With Lawessons reagent; phosphorus tribromide; N,N-dimethyl-formamide; lithium diisopropyl amide; In tetrahydrofuran; n-heptane; dichloromethane; ethylbenzene; toluene;
DOI:10.1002/1522-2675(200210)85:10<3422::AID-HLCA3422>3.0.CO;2-N