N-[(2R,3S)-5-Hydroxy-2-(1-hydroxy-1-methyl-ethyl)-tetrahydro-furan-3-yl]-benzamide

Base Information

Chemical Name:N-[(2R,3S)-5-Hydroxy-2-(1-hydroxy-1-methyl-ethyl)-tetrahydro-furan-3-yl]-benzamide
CAS No.:82010-47-7
Molecular Formula:C₁₄H₁₉NO₄
Molecular Weight:265.309
Hs Code.:

Synonyms:N-[(2R,3S)-5-Hydroxy-2-(1-hydroxy-1-methyl-ethyl)-tetrahydro-furan-3-yl]-benzamide

Suppliers and Price of N-[(2R,3S)-5-Hydroxy-2-(1-hydroxy-1-methyl-ethyl)-tetrahydro-furan-3-yl]-benzamide

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 N-[(2R,3S)-5-Hydroxy-2-(1-hydroxy-1-methyl-ethyl)-tetrahydro-furan-3-yl]-benzamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-[(2R,3S)-5-Hydroxy-2-(1-hydroxy-1-methyl-ethyl)-tetrahydro-furan-3-yl]-benzamide

There total 6 articles about N-[(2R,3S)-5-Hydroxy-2-(1-hydroxy-1-methyl-ethyl)-tetrahydro-furan-3-yl]-benzamide 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: 80.0%

: 82010-44-4
(3R,4R)-3-(benzoylamino)-4,5-dihydroxy-5-methylhexanoic acid γ-lactone

: 82010-47-7
N-[(2R,3S)-5-Hydroxy-2-(1-hydroxy-1-methyl-ethyl)-tetrahydro-furan-3-yl]-benzamide

Guidance literature:: With diisobutylaluminium hydride; In tetrahydrofuran; toluene; at -40 ℃; for 3h;
DOI:10.1021/jo00138a018

Reference yield:

: 82010-35-3
(S)-3,3-Dimethyl-1,4-dioxa-spiro[4.5]decane-2-carbaldehyde

: 82010-47-7
N-[(2R,3S)-5-Hydroxy-2-(1-hydroxy-1-methyl-ethyl)-tetrahydro-furan-3-yl]-benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: benzoic acid / diethyl ether / 4 h / Heating

2: NH₃ / 120 h / Ambient temperature

3: 1.) 2 N HCl, 2.) NaHCO₃ / 1.) ether, reflux, 2 h, 2.) water, acetone, RT, 5 h

4: 80 percent / diisobutylaluminium hydride / tetrahydrofuran; toluene / 3 h / -40 °C

With hydrogenchloride; ammonia; diisobutylaluminium hydride; sodium hydrogencarbonate; benzoic acid; In tetrahydrofuran; diethyl ether; toluene;
DOI:10.1021/jo00138a018

Reference yield:

: 82010-37-5
(S)-3,3-Dimethyl-1,4-dioxa-spiro[4.5]decane-2-carboxylic acid

: 82010-47-7
N-[(2R,3S)-5-Hydroxy-2-(1-hydroxy-1-methyl-ethyl)-tetrahydro-furan-3-yl]-benzamide

Guidance literature:: Multi-step reaction with 6 steps

1: LiAlH₄ / diethyl ether / 2 h / Heating

2: pyridinium chlorochromate, sodium acetate / CH₂Cl₂ / 3 h / Ambient temperature

3: benzoic acid / diethyl ether / 4 h / Heating

4: NH₃ / 120 h / Ambient temperature

5: 1.) 2 N HCl, 2.) NaHCO₃ / 1.) ether, reflux, 2 h, 2.) water, acetone, RT, 5 h

6: 80 percent / diisobutylaluminium hydride / tetrahydrofuran; toluene / 3 h / -40 °C

With hydrogenchloride; lithium aluminium tetrahydride; ammonia; sodium acetate; diisobutylaluminium hydride; sodium hydrogencarbonate; benzoic acid; pyridinium chlorochromate; In tetrahydrofuran; diethyl ether; dichloromethane; toluene;
DOI:10.1021/jo00138a018