((2S,3R,4S)-4-amino-2-(fluoromethyl)-4-(2-fluorophenyl)tetrahydrofuran-3-yl)methanol

Base Information

Chemical Name:((2S,3R,4S)-4-amino-2-(fluoromethyl)-4-(2-fluorophenyl)tetrahydrofuran-3-yl)methanol
CAS No.:1391001-92-5
Molecular Formula:C₁₂H₁₅F₂NO₂
Molecular Weight:243.253
Hs Code.:

Synonyms:((2S,3R,4S)-4-amino-2-(fluoromethyl)-4-(2-fluorophenyl)tetrahydrofuran-3-yl)methanol

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Chemical Property of ((2S,3R,4S)-4-amino-2-(fluoromethyl)-4-(2-fluorophenyl)tetrahydrofuran-3-yl)methanol

Chemical Property:

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Technology Process of ((2S,3R,4S)-4-amino-2-(fluoromethyl)-4-(2-fluorophenyl)tetrahydrofuran-3-yl)methanol

There total 8 articles about ((2S,3R,4S)-4-amino-2-(fluoromethyl)-4-(2-fluorophenyl)tetrahydrofuran-3-yl)methanol 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:

: 1391001-88-9
(S)-2-((1-fluorobut-3-en-2-yl)oxy)-N-methoxy-N-methylacetamide

: 1391001-92-5
((2S,3R,4S)-4-amino-2-(fluoromethyl)-4-(2-fluorophenyl)tetrahydrofuran-3-yl)methanol

Guidance literature:: Multi-step reaction with 4 steps

1.1: n-butyllithium / hexane; tetrahydrofuran / -78 - -60 °C / Inert atmosphere

1.2: -78 - -60 °C

2.1: hydroxylamine hydrochloride; sodium acetate / methanol / 1.5 h / 50 °C

3.1: hydroquinone / xylene / 5 h / Reflux

4.1: zinc; acetic acid / 0 - 20 °C

With n-butyllithium; hydroxylamine hydrochloride; sodium acetate; acetic acid; hydroquinone; zinc; In tetrahydrofuran; methanol; hexane; xylene;

Reference yield:

: 1391001-89-0
(S)-2-((1-fluorobut-3-en-2-yl)oxy)-1-(2-fluorophenyl)ethanone

: 1391001-92-5
((2S,3R,4S)-4-amino-2-(fluoromethyl)-4-(2-fluorophenyl)tetrahydrofuran-3-yl)methanol

Guidance literature:: Multi-step reaction with 3 steps

1: hydroxylamine hydrochloride; sodium acetate / methanol / 1.5 h / 50 °C

2: hydroquinone / xylene / 5 h / Reflux

3: zinc; acetic acid / 0 - 20 °C

With hydroxylamine hydrochloride; sodium acetate; acetic acid; hydroquinone; zinc; In methanol; xylene;

Reference yield:

: 1391001-87-8
tert-butyl (S)-2-((1-fluorobut-3-en-2-yl)oxy)acetate

: 1391001-92-5
((2S,3R,4S)-4-amino-2-(fluoromethyl)-4-(2-fluorophenyl)tetrahydrofuran-3-yl)methanol

Guidance literature:: Multi-step reaction with 6 steps

1.1: formic acid / 0 - 20 °C

2.1: 1,1'-carbonyldiimidazole / dichloromethane / 3 - 20 °C

2.2: 3 - 20 °C

3.1: n-butyllithium / hexane; tetrahydrofuran / -78 - -60 °C / Inert atmosphere

3.2: -78 - -60 °C

4.1: hydroxylamine hydrochloride; sodium acetate / methanol / 1.5 h / 50 °C

5.1: hydroquinone / xylene / 5 h / Reflux

6.1: zinc; acetic acid / 0 - 20 °C

With n-butyllithium; formic acid; hydroxylamine hydrochloride; sodium acetate; acetic acid; hydroquinone; 1,1'-carbonyldiimidazole; zinc; In tetrahydrofuran; methanol; hexane; dichloromethane; xylene;