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(S)-1,2,3,4-tetrahydro-5-methoxy-N-propyl-naphthalen-2-ammonium (R)-2-(2-chlorophenyl)-2-hydroxyacetate
(S)-(-)-(5-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)propylamine hydrochloride
| Conditions | Yield |
|---|---|
|
With hydrogenchloride; In tetrahydrofuran; water; at 65 ℃; for 0.25h;
|
94% |
|
With hydrogenchloride; In tetrahydrofuran; water; at 60 - 65 ℃; for 2.25h; Reflux;
|
94% |
(S)-1,2,3,4-tetrahydro-5-methoxy-N-propyl-naphthalen-2-ammonium (S)-2-hydroxy-3-phenylpropionate
(S)-(-)-(5-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)propylamine hydrochloride
| Conditions | Yield |
|---|---|
|
(S)-1,2,3,4-tetrahydro-5-methoxy-N-propyl-naphthalen-2-ammonium (S)-2-hydroxy-3-phenylpropionate; With sodium hydroxide; In 2-methyltetrahydrofuran; water; at 20 ℃;
With hydrogenchloride; In 2-methyltetrahydrofuran; water; at 60 ℃;
|
84% |
|
(S)-1,2,3,4-tetrahydro-5-methoxy-N-propyl-naphthalen-2-ammonium (S)-2-hydroxy-3-phenylpropionate; With sodium hydroxide; In 2-methyltetrahydrofuran; water; at 20 ℃;
With hydrogenchloride; In 2-methyltetrahydrofuran; water; at 60 ℃;
|
84% |
The CAS number of (S)-1,2,3,4-Tetrahydro-5-methoxy-N-propyl-2-naphthalenamine hydrochloride is 93601-86-6.
More information of (S)-1,2,3,4-Tetrahydro-5-methoxy-N-propyl-2-naphthalenamine hydrochloride 93601-86-6 are:
|
CAS Number |
93601-86-6 |
|
Density |
1.19g/cm3 at 20℃ |
|
Vapor Pressure |
0-0Pa at 20-25℃ |
|
HS CODE |
2932999099 |
|
PSA |
21.26000 |
|
LogP |
3.74500 |
Synonyms for (S)-1,2,3,4-Tetrahydro-5-methoxy-N-propyl-2-naphthalenamine hydrochloride 93601-86-6:(2S)-5-Methoxy-N-propyl-1,2,3,4-tetrahydronaphthalen-2-aminhydrochlorid(1:1);
The chemical formula of (S)-1,2,3,4-Tetrahydro-5-methoxy-N-propyl-2-naphthalenamine hydrochloride is C14H21NO.HCl which containing 14 Carbon atoms,22 Hydrogen atoms,1 Nitrogen atoms and 1 Chlorine atoms,and the molecular weight of (S)-1,2,3,4-Tetrahydro-5-methoxy-N-propyl-2-naphthalenamine hydrochloride is 255.788.
Relevant articles related to (S)-1,2,3,4-Tetrahydro-5-methoxy-N-propyl-2-naphthalenamine hydrochloride:
|
Article |
Source |
|
Enantioselective Synthesis of β-Aminotetralins via Chiral Phosphoric Acid-catalyzed Reductive Amination of β-Tetralones |
Park, Do Young,Kim, Kyung-Hee,Cheon, Cheol-Hong supporting information, p. 462 - 467 (2017/12/07) |
|
Novel Process for the Preparation of Nitrogen Substituted Aminotetralins Derivatives |
- , (2013/05/08) |
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