(RS)-4-[N-(tert-butyloxycarbonyl)-N-methylamino]-3-benzyloxy-4,5,6,7-tetrahydrobenzo[d]isoxazole

Base Information

Chemical Name:(RS)-4-[N-(tert-butyloxycarbonyl)-N-methylamino]-3-benzyloxy-4,5,6,7-tetrahydrobenzo[d]isoxazole
CAS No.:847233-15-2
Molecular Formula:C₂₀H₂₆N₂O₄
Molecular Weight:358.437
Hs Code.:

Synonyms:(RS)-4-[N-(tert-butyloxycarbonyl)-N-methylamino]-3-benzyloxy-4,5,6,7-tetrahydrobenzo[d]isoxazole

Suppliers and Price of (RS)-4-[N-(tert-butyloxycarbonyl)-N-methylamino]-3-benzyloxy-4,5,6,7-tetrahydrobenzo[d]isoxazole

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 (RS)-4-[N-(tert-butyloxycarbonyl)-N-methylamino]-3-benzyloxy-4,5,6,7-tetrahydrobenzo[d]isoxazole

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (RS)-4-[N-(tert-butyloxycarbonyl)-N-methylamino]-3-benzyloxy-4,5,6,7-tetrahydrobenzo[d]isoxazole

There total 1 articles about (RS)-4-[N-(tert-butyloxycarbonyl)-N-methylamino]-3-benzyloxy-4,5,6,7-tetrahydrobenzo[d]isoxazole 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: 39.0%

: 100-39-0
benzyl bromide

: 182317-21-1
(RS)-4-[N-(tert-butyloxycarbonyl)methylamino]-3-hydroxy-4,5,6,7-tetrahydro-1,2-benzisoxazole

: 847233-15-2
(RS)-4-[N-(tert-butyloxycarbonyl)-N-methylamino]-3-benzyloxy-4,5,6,7-tetrahydrobenzo[d]isoxazole

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 40 ℃;
DOI:10.1016/j.bmc.2004.10.029

Reference yield: 90.0%

: 847233-15-2
(RS)-4-[N-(tert-butyloxycarbonyl)-N-methylamino]-3-benzyloxy-4,5,6,7-tetrahydrobenzo[d]isoxazole

: (RS)-4-N-methylamino-3-benzyloxy-4,5,6,7-tetrahydrobenzo[d]isoxazole hydrochloride

Guidance literature:: With hydrogenchloride; In ethanol; at 45 ℃; for 2h;
DOI:10.1016/j.bmc.2004.10.029

Reference yield:

: 847233-15-2
(RS)-4-[N-(tert-butyloxycarbonyl)-N-methylamino]-3-benzyloxy-4,5,6,7-tetrahydrobenzo[d]isoxazole

: 847233-16-3
(RS)-4-[N-(1,1-diphenylbul-1-en-4-yl)-N-methylamino]-3-benzyloxy-4,5,6,7-tetrahydrobenzo[d]isoxazole

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / hydrochloric acid / ethanol / 2 h / 45 °C

2: 85 percent / K₂CO₃; NaI / dimethylformamide / 48 h / 120 °C

With hydrogenchloride; potassium carbonate; sodium iodide; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2004.10.029