((1S,3S,4R)-1-allyl-4-(benzyloxy)-7-fluoro-1,2,3,4-tetrahydroisoquinolin-3-yl)methanol

Base Information

Chemical Name:((1S,3S,4R)-1-allyl-4-(benzyloxy)-7-fluoro-1,2,3,4-tetrahydroisoquinolin-3-yl)methanol
CAS No.:1307772-46-8
Molecular Formula:C₂₀H₂₂FNO₂
Molecular Weight:327.399
Hs Code.:

Synonyms:((1S,3S,4R)-1-allyl-4-(benzyloxy)-7-fluoro-1,2,3,4-tetrahydroisoquinolin-3-yl)methanol

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of ((1S,3S,4R)-1-allyl-4-(benzyloxy)-7-fluoro-1,2,3,4-tetrahydroisoquinolin-3-yl)methanol

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Technology Process of ((1S,3S,4R)-1-allyl-4-(benzyloxy)-7-fluoro-1,2,3,4-tetrahydroisoquinolin-3-yl)methanol

There total 7 articles about ((1S,3S,4R)-1-allyl-4-(benzyloxy)-7-fluoro-1,2,3,4-tetrahydroisoquinolin-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: 96.0%

: 1307772-10-6
(9H-fluoren-9-yl)methyl (1S,3S,4R)-1-allyl-4-(benzyloxy)-7-fluoro-3-(hydroxymethyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

: 1307772-46-8
((1S,3S,4R)-1-allyl-4-(benzyloxy)-7-fluoro-1,2,3,4-tetrahydroisoquinolin-3-yl)methanol

Guidance literature:: With piperidine; In N,N-dimethyl-formamide; for 0.166667h;
DOI:10.1002/chem.201002938

Reference yield:

: 1307771-17-0
tert-butyl (4S)-4-((R)-(2-(1,3-dioxan-2-yl)-4-fluorophenyl)(benzyloxy)methyl)-2,2-dimethyloxazolidine-3-carboxylate

: 1307772-46-8
((1S,3S,4R)-1-allyl-4-(benzyloxy)-7-fluoro-1,2,3,4-tetrahydroisoquinolin-3-yl)methanol

Guidance literature:: Multi-step reaction with 4 steps

1: hydrogenchloride / tetrahydrofuran; water / 2 h / 20 °C

2: dichloromethane / 20 °C

3: ytterbium(III) triflate / dichloromethane / -20 - 20 °C

4: piperidine / N,N-dimethyl-formamide / 0.17 h

With piperidine; hydrogenchloride; ytterbium(III) triflate; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1002/chem.201002938

Reference yield:

: C₂₁H₃₀FNO₆

: 1307772-46-8
((1S,3S,4R)-1-allyl-4-(benzyloxy)-7-fluoro-1,2,3,4-tetrahydroisoquinolin-3-yl)methanol

Guidance literature:: Multi-step reaction with 5 steps

1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 3 h / 0 °C

2: hydrogenchloride / tetrahydrofuran; water / 2 h / 20 °C

3: dichloromethane / 20 °C

4: ytterbium(III) triflate / dichloromethane / -20 - 20 °C

5: piperidine / N,N-dimethyl-formamide / 0.17 h

With piperidine; hydrogenchloride; sodium hydride; ytterbium(III) triflate; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; mineral oil;
DOI:10.1002/chem.201002938