(1R,2S)-1,2-Bis-(3-benzyloxy-4-methoxy-phenyl)-2-[(2,2-dimethoxy-ethyl)-methyl-amino]-ethanol

Base Information

Chemical Name:(1R,2S)-1,2-Bis-(3-benzyloxy-4-methoxy-phenyl)-2-[(2,2-dimethoxy-ethyl)-methyl-amino]-ethanol
CAS No.:133343-24-5
Molecular Formula:C₃₅H₄₁NO₇
Molecular Weight:587.713
Hs Code.:

Synonyms:(1R,2S)-1,2-Bis-(3-benzyloxy-4-methoxy-phenyl)-2-[(2,2-dimethoxy-ethyl)-methyl-amino]-ethanol

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Chemical Property of (1R,2S)-1,2-Bis-(3-benzyloxy-4-methoxy-phenyl)-2-[(2,2-dimethoxy-ethyl)-methyl-amino]-ethanol

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Technology Process of (1R,2S)-1,2-Bis-(3-benzyloxy-4-methoxy-phenyl)-2-[(2,2-dimethoxy-ethyl)-methyl-amino]-ethanol

There total 15 articles about (1R,2S)-1,2-Bis-(3-benzyloxy-4-methoxy-phenyl)-2-[(2,2-dimethoxy-ethyl)-methyl-amino]-ethanol 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: 79.0%

: 133343-21-2,135637-65-9,140851-45-2
(2R,3R)-2,3-Bis-(3-benzyloxy-4-methoxy-phenyl)-oxirane

: 122-07-6
N-(methyl)aminoacetaldehyde dimethyl acetal

: 133343-24-5,140687-77-0,140851-47-4
(1R,2S)-1,2-Bis-(3-benzyloxy-4-methoxy-phenyl)-2-[(2,2-dimethoxy-ethyl)-methyl-amino]-ethanol

Guidance literature:: With silica gel; In butan-1-ol; for 2h; r.t. to 90 deg C;
DOI:10.1016/S0040-4039(00)97306-4

Reference yield:

: 133343-20-1
3,3'-Dibenzyloxy-4,4'-dimethoxystilben

: 133343-24-5,140687-77-0,140851-47-4
1,2-Bis-(3-benzyloxy-4-methoxy-phenyl)-2-[(2,2-dimethoxy-ethyl)-methyl-amino]-ethanol

Guidance literature:: Multi-step reaction with 4 steps

1: OsCl₃, dihydroquinidine 4-chlorobenzoate, N-methylmorpholine N-oxide / acetone; H₂O / 24 h / Ambient temperature

2: SOCl₂, Et₃N / diethyl ether / 1 h / 0 deg C to r.t.

3: RuCl₃, NaOCl / acetonitrile

4: 2 h / r.t. to 130 deg C

With ruthenium trichloride; sodium hypochlorite; thionyl chloride; dihydroquinidine 4-chlorobenzoate; osmium (III) chloride; 4-methylmorpholine N-oxide; triethylamine; In diethyl ether; water; acetone; acetonitrile;
DOI:10.1016/S0040-4039(00)97306-4

Reference yield:

: 133343-20-1
3,3'-Dibenzyloxy-4,4'-dimethoxystilben

: 133343-24-5
(1R,2S)-1,2-Bis-(3-benzyloxy-4-methoxy-phenyl)-2-[(2,2-dimethoxy-ethyl)-methyl-amino]-ethanol

Guidance literature:: Multi-step reaction with 4 steps

1: OsCl₃, dihydroquinidine 4-chlorobenzoate, N-methylmorpholine N-oxide / acetone; H₂O / 24 h / Ambient temperature

2: SOCl₂, Et₃N / diethyl ether / 1 h / 0 deg C to r.t.

3: RuCl₃, NaOCl / acetonitrile

4: 2 h / r.t. to 130 deg C

With ruthenium trichloride; sodium hypochlorite; thionyl chloride; dihydroquinidine 4-chlorobenzoate; osmium (III) chloride; 4-methylmorpholine N-oxide; triethylamine; In diethyl ether; water; acetone; acetonitrile;
DOI:10.1016/S0040-4039(00)97306-4