Benzoic acid (2R,3S,6R)-6-tert-butoxy-3-(1-methoxy-1-methyl-ethoxy)-tetrahydro-pyran-2-ylmethyl ester

Base Information

Chemical Name:Benzoic acid (2R,3S,6R)-6-tert-butoxy-3-(1-methoxy-1-methyl-ethoxy)-tetrahydro-pyran-2-ylmethyl ester
CAS No.:107108-68-9
Molecular Formula:C₂₁H₃₂O₆
Molecular Weight:380.481
Hs Code.:

Synonyms:Benzoic acid (2R,3S,6R)-6-tert-butoxy-3-(1-methoxy-1-methyl-ethoxy)-tetrahydro-pyran-2-ylmethyl ester

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Chemical Property of Benzoic acid (2R,3S,6R)-6-tert-butoxy-3-(1-methoxy-1-methyl-ethoxy)-tetrahydro-pyran-2-ylmethyl ester

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Technology Process of Benzoic acid (2R,3S,6R)-6-tert-butoxy-3-(1-methoxy-1-methyl-ethoxy)-tetrahydro-pyran-2-ylmethyl ester

There total 6 articles about Benzoic acid (2R,3S,6R)-6-tert-butoxy-3-(1-methoxy-1-methyl-ethoxy)-tetrahydro-pyran-2-ylmethyl 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: 86.0%

: 116-11-0
2-Methoxypropene

: 107123-48-8
Benzoic acid (2R,3S,6R)-6-tert-butoxy-3-hydroxy-tetrahydro-pyran-2-ylmethyl ester

: 107108-68-9
Benzoic acid (2R,3S,6R)-6-tert-butoxy-3-(1-methoxy-1-methyl-ethoxy)-tetrahydro-pyran-2-ylmethyl ester

Guidance literature:: With camphor-10-sulfonic acid; In dichloromethane; for 1.5h; Ambient temperature;
DOI:10.1016/S0040-4020(01)90575-7

Reference yield:

: 69247-20-7,149279-18-5,23339-25-5
tert-butyl 4,6-di-O-acetyl-2,3-dideoxy-α-D-erythrohex-2-enopyranoside

: 107108-68-9
Benzoic acid (2R,3S,6R)-6-tert-butoxy-3-(1-methoxy-1-methyl-ethoxy)-tetrahydro-pyran-2-ylmethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: H₂ / Pd-C(5percent) / ethyl acetate / 12 h

2: Et₃N, H₂O / methanol / Ambient temperature

3: CH₂Cl₂ / 0 deg C, then room temp., overnight

4: 86 percent / CSA / CH₂Cl₂ / 1.5 h / Ambient temperature

With camphor-10-sulfonic acid; water; hydrogen; triethylamine; 5%-palladium/activated carbon; In methanol; dichloromethane; ethyl acetate;
DOI:10.1016/S0040-4020(01)90575-7

Reference yield:

: 2873-29-2
D-glucal triacetate

: 107108-68-9
Benzoic acid (2R,3S,6R)-6-tert-butoxy-3-(1-methoxy-1-methyl-ethoxy)-tetrahydro-pyran-2-ylmethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 97 percent / BF₃-Et₂O / 1.67 h / Ambient temperature

2: H₂ / Pd-C(5percent) / ethyl acetate / 12 h

3: Et₃N, H₂O / methanol / Ambient temperature

4: CH₂Cl₂ / 0 deg C, then room temp., overnight

5: 86 percent / CSA / CH₂Cl₂ / 1.5 h / Ambient temperature

With camphor-10-sulfonic acid; boron trifluoride diethyl etherate; water; hydrogen; triethylamine; 5%-palladium/activated carbon; In methanol; dichloromethane; ethyl acetate;
DOI:10.1016/S0040-4020(01)90575-7