(R)-<(2RS,5S)-5-<(2R,5R,6S)-5-benzyloxy-5-ethyl-6-methyltetrahydropyran-2-yl>-2-methoxy-5-methyltetrahydrofuran-2-yl>-2-(4-methoxybenzyloxy)ethan-1-ol

Base Information

Chemical Name:(R)-<(2RS,5S)-5-<(2R,5R,6S)-5-benzyloxy-5-ethyl-6-methyltetrahydropyran-2-yl>-2-methoxy-5-methyltetrahydrofuran-2-yl>-2-(4-methoxybenzyloxy)ethan-1-ol
CAS No.:126365-82-0
Molecular Formula:C₃₁H₄₄O₇
Molecular Weight:528.686
Hs Code.:

(R)-<(2RS,5S)-5-<(2R,5R,6S)-5-benzyloxy-5-ethyl-6-methyltetrahydropyran-2-yl>-2-methoxy-5-methyltetrahydrofuran-2-yl>-2-(4-methoxybenzyloxy)ethan-1-ol

Synonyms:

Suppliers and Price of (R)-<(2RS,5S)-5-<(2R,5R,6S)-5-benzyloxy-5-ethyl-6-methyltetrahydropyran-2-yl>-2-methoxy-5-methyltetrahydrofuran-2-yl>-2-(4-methoxybenzyloxy)ethan-1-ol

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)-<(2RS,5S)-5-<(2R,5R,6S)-5-benzyloxy-5-ethyl-6-methyltetrahydropyran-2-yl>-2-methoxy-5-methyltetrahydrofuran-2-yl>-2-(4-methoxybenzyloxy)ethan-1-ol

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (R)-<(2RS,5S)-5-<(2R,5R,6S)-5-benzyloxy-5-ethyl-6-methyltetrahydropyran-2-yl>-2-methoxy-5-methyltetrahydrofuran-2-yl>-2-(4-methoxybenzyloxy)ethan-1-ol

There total 10 articles about (R)-<(2RS,5S)-5-<(2R,5R,6S)-5-benzyloxy-5-ethyl-6-methyltetrahydropyran-2-yl>-2-methoxy-5-methyltetrahydrofuran-2-yl>-2-(4-methoxybenzyloxy)ethan-1-ol 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: 95.0%

: 126365-81-9
(2S,3R,6R)-3-Benzyloxy-3-ethyl-6-{(S)-5-methoxy-5-[(R)-1-(4-methoxy-benzyloxy)-2-(1-methoxy-1-methyl-ethoxy)-ethyl]-2-methyl-tetrahydro-furan-2-yl}-2-methyl-tetrahydro-pyran

: 126365-82-0,126455-54-7
(R)-<(2RS,5S)-5-<(2R,5R,6S)-5-benzyloxy-5-ethyl-6-methyltetrahydropyran-2-yl>-2-methoxy-5-methyltetrahydrofuran-2-yl>-2-(4-methoxybenzyloxy)ethan-1-ol

Guidance literature:: With methanol; camphor-10-sulfonic acid; for 0.333333h; Ambient temperature;
DOI:10.1248/cpb.37.1726

Reference yield:

: 126394-14-7
(E)-1-((2R,5R,6S)-5-Benzyloxy-5-ethyl-6-methyl-tetrahydro-pyran-2-yl)-3-[(4R,5R)-5-(4-methoxy-benzyloxy)-2,2-dimethyl-[1,3]dioxan-4-yl]-propenone

: 126365-82-0,126455-54-7
(R)-<(2RS,5S)-5-<(2R,5R,6S)-5-benzyloxy-5-ethyl-6-methyltetrahydropyran-2-yl>-2-methoxy-5-methyltetrahydrofuran-2-yl>-2-(4-methoxybenzyloxy)ethan-1-ol

Guidance literature:: Multi-step reaction with 6 steps

1: 98 percent / hydrogen / 10percent Pd/C / ethyl acetate / 0.17 h

2: 87 percent / diethyl ether / 2 h / -93 °C

3: 96 percent / 1N HCl / tetrahydrofuran / 0.5 h / Ambient temperature

4: 100 percent / imidazole / CH₂Cl₂ / 0.5 h / Ambient temperature

5: 1) DMSO, (COCl)2, 2) Et₃N / 1) CH₂Cl₂, -70 deg C, 2) CH₂Cl₂, -70 to 0 deg C

6: CSA / 0.08 h / Ambient temperature

With 1H-imidazole; hydrogenchloride; oxalyl dichloride; camphor-10-sulfonic acid; hydrogen; dimethyl sulfoxide; triethylamine; palladium on activated charcoal; In tetrahydrofuran; diethyl ether; dichloromethane; ethyl acetate;
DOI:10.1248/cpb.37.1705

Reference yield:

: 113981-32-1
(4R,5R)-1-<(2R,5R,6S)-5-benzyloxy-5-ethyl-6-methyltetrahydropyran-2-yl>-4,6-isopropylidenedioxy-5-(4-methoxybenzyloxy)hexan-1-one

: 126365-82-0,126455-54-7
(R)-<(2RS,5S)-5-<(2R,5R,6S)-5-benzyloxy-5-ethyl-6-methyltetrahydropyran-2-yl>-2-methoxy-5-methyltetrahydrofuran-2-yl>-2-(4-methoxybenzyloxy)ethan-1-ol

Guidance literature:: Multi-step reaction with 5 steps

1: 87 percent / diethyl ether / 2 h / -93 °C

2: 96 percent / 1N HCl / tetrahydrofuran / 0.5 h / Ambient temperature

3: 100 percent / imidazole / CH₂Cl₂ / 0.5 h / Ambient temperature

4: 1) DMSO, (COCl)2, 2) Et₃N / 1) CH₂Cl₂, -70 deg C, 2) CH₂Cl₂, -70 to 0 deg C

5: CSA / 0.08 h / Ambient temperature

With 1H-imidazole; hydrogenchloride; oxalyl dichloride; camphor-10-sulfonic acid; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1248/cpb.37.1705