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inquiryOur company was built in 2009 with an ISO certificate.In the past 6 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.O
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inquiryName: L-(+)-Prolinol Synonyms: (S)-(+)-2-Hydroxymethylpyrrolidine CAS:23356-96-9 MF: C5H12NO Appearance: white powder Storage:Store in cool and dry place, away from sun light. Package: 25kgs/drum Application: APIs Transportation:By sea or by air
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inquiryL-(+)-Prolinol CAS: 23356-96-9 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic intermedi
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inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
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inquiryProduct Detail Minimum Order Qty. 10 Gram
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inquiryBest quality & Attractive price & Professional service; Trial & Pilot & Commercial Hisunny Chemical is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality intermediates, specia
ProName:Top sale 23356-96-9 L-(+)-Prolinol wit... CasNo:23356-96-9 Molecular Formula:C5H11NO Appearance:White or off-white Solid Application:pharmaceutical intermediates DeliveryTime:5-7days PackAge:25kg/bag or follow your requirement Port:S
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inquiryL-proline
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
Stage #1: L-proline With lithium aluminium tetrahydride In tetrahydrofuran for 1.25h; Heating / reflux; Stage #2: With potassium hydroxide In tetrahydrofuran; water for 1.25h; Heating / reflux; | 100% |
Stage #1: L-proline With lithium aluminium tetrahydride In tetrahydrofuran Inert atmosphere; Cooling with ice; Reflux; Stage #2: With potassium hydroxide In tetrahydrofuran at 20℃; Reflux; | 99% |
With lithium aluminium tetrahydride In tetrahydrofuran at 0℃; for 72.5h; Reflux; | 99% |
methanol
B
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With hydrogenchloride Heating; | A n/a B 96% |
methanol
B
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With hydrogenchloride Heating; | A n/a B 96% |
methanol
B
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With hydrogenchloride Heating; | A n/a B 96% |
methanol
B
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With hydrogenchloride Heating; | A n/a B 96% |
A
(rac)-N-benzyl-N-methylalanine
B
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With hydrogenchloride In methanol Heating; | A n/a B 96% |
A
2-(benzyl(methyl)amino)-3-methylbutanoic acid
B
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With hydrogenchloride In methanol Heating; | A n/a B 96% |
A
(rac)-N-benzyl-N-methylphenylalanine
B
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With hydrogenchloride In methanol Heating; | A n/a B 96% |
B
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With hydrogenchloride In methanol Heating; | A n/a B 96% |
L-Pyroglutamic acid
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With hydrogen; acetic acid In water at 100℃; under 52505.3 Torr; for 20h; Pressure; Temperature; Reagent/catalyst; Time; Autoclave; | 95% |
(-)-(2R)-[(2S)-(hydroxymethyl)pyrrolidin-1-yl]-2-phenylethanol
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In methanol under 760 Torr; for 2h; Ambient temperature; | 90% |
With hydrogen; palladium on activated charcoal In methanol at 20℃; under 760 Torr; for 2h; Hydrogenolysis; debenzylation; | 90% |
methyl (2S)-pyrrolidine carboxylate
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran at 20℃; Inert atmosphere; Reflux; | 90% |
With lithium aluminium tetrahydride In tetrahydrofuran at 20℃; for 1h; Cooling with ice; Inert atmosphere; | 86.5% |
N-(tert-butoxycarbonyl)-L-prolinol
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With trifluoroacetic acid | 90% |
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With methanol; iodine for 3h; Heating; | 82% |
(1’R,2S)-[1-(2’-benzyloxy-1’-phenylethyl)pyrrolidin-2-yl]methanol
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With 10 wt% Pd(OH)2 on carbon; hydrogen In methanol at 20℃; under 2280.15 Torr; for 15h; | 74.1% |
(5aS,10aS)-octahydrodipyrrolo[1,2-a:1',2'-d]pyrazine-5,10-dione
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With C24H20ClN2OPRu; potassium tert-butylate; hydrogen In tetrahydrofuran at 110℃; under 2280.15 - 30402 Torr; for 48h; Inert atmosphere; Schlenk technique; Autoclave; | 67% |
B
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With sodium bis(2-methoxyethoxy)aluminium dihydride In toluene | A 65% B n/a |
(2S,1'S)-2-Hydroxymethyl-N-1'-(2-methoxyphenyl)propyl-1-pyrrolidinecarboxamide
A
(S)-N-Methyl-1-(2-methoxyphenyl)propylamine
B
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With sodium bis(2-methoxyethoxy)aluminium dihydride In toluene | A 57% B n/a |
2-hydroxymethylpyrrolidine
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
36% |
L-proline methyl ester monohydrochloride
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With carbonylhydrido(tetrahydroborato)[bis(2-diphenylphosphinoethyl)-amino]ruthenium(II); potassium methanolate; hydrogen In tetrahydrofuran at 100℃; under 75007.5 Torr; Autoclave; | 25% |
With lithium aluminium tetrahydride In tetrahydrofuran for 2h; Heating; |
ethyl (2S)-pyrrolidine-2-carboxylate
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride; diethyl ether | |
Stage #1: ethyl (2S)-pyrrolidine-2-carboxylate With sodium tetrahydroborate; lithium chloride In methanol at 5 - 25℃; for 4.5h; Large scale; Stage #2: With hydrogenchloride In methanol; water at 20 - 25℃; for 2h; Large scale; | 117 kg |
N-Cbz-Prolinol
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal Yield given; |
(2S,5S)-2-Hydroxymethyl-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-pyrrolidine-1-carboxylic acid benzyl ester
A
thymin
B
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In ethanol; water |
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With hydrogenchloride In water at 85 - 90℃; for 48h; Yield given; |
(S)-(1-(4-methoxybenzyl)pyrrolidin-2-yl)methanol
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With hydrogenchloride; hydrogen; palladium on activated charcoal In methanol under 760 Torr; |
diethyl ether
(S)-butyl 5-oxopyrrolidine-2-carboxylate
(S)-1-Pyrrolidin-2-yl-methanol
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride; diethyl ether |
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride; diethyl ether |
di-tert-butyl dicarbonate
(S)-1-Pyrrolidin-2-yl-methanol
N-(tert-butoxycarbonyl)-L-prolinol
Conditions | Yield |
---|---|
With triethylamine In ethyl acetate at 0 - 20℃; for 11.5h; | 100% |
With triethylamine In ethyl acetate at 0 - 20℃; for 11.5h; | 100% |
With sodium hydrogencarbonate In tetrahydrofuran; water at 0 - 20℃; Inert atmosphere; | 100% |
oxalic acid diethyl ester
(S)-1-Pyrrolidin-2-yl-methanol
1,2-Bis-((S)-2-hydroxymethyl-pyrrolidin-1-yl)-ethane-1,2-dione
Conditions | Yield |
---|---|
0 degC-room temp, 2 h, room temp; | 100% |
chloro-diphenylphosphine
(S)-1-Pyrrolidin-2-yl-methanol
(S)-(N-diphenylphosphino)(2-diphenylphosphinoxymethyl)pyrrolidine
Conditions | Yield |
---|---|
With triethylamine In toluene Ambient temperature; | 100% |
With triethylamine In toluene at 0℃; for 16h; Yield given; | |
With triethylamine In toluene |
(S)-1-Pyrrolidin-2-yl-methanol
formic acid ethyl ester
(S)-(-)-1-Formyl-2-(hydroxymethyl)pyrrolidine
Conditions | Yield |
---|---|
at 50℃; | 100% |
2-Chloroquinoline
(S)-1-Pyrrolidin-2-yl-methanol
(S)-2-(hydroxymethyl)-1-(quinolin-2-yl)pyrrolidine
Conditions | Yield |
---|---|
at 160℃; for 4h; | 100% |
Methyl formate
(S)-1-Pyrrolidin-2-yl-methanol
(S)-(-)-1-Formyl-2-(hydroxymethyl)pyrrolidine
Conditions | Yield |
---|---|
Inert atmosphere; | 100% |
In tetrahydrofuran at 0℃; for 2h; | |
at 0℃; for 0.833333h; |
(S)-1-Pyrrolidin-2-yl-methanol
3-[4-((2S)-2-hydroxymethylpyrrolidine-1-carbonyl)-2-methoxy-5-nitrophenoxy]propionic acid benzyl ester
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at -30 - 20℃; | 100% |
With triethylamine In dichloromethane at -50 - 20℃; for 18h; |
(S)-1-Pyrrolidin-2-yl-methanol
4-[4-((2S)-2-hydroxymethylpyrrolidine-1-carbonyl)-2-methoxy-5-nitrophenoxy]butanoic acid methyl ester
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at -30 - 20℃; | 100% |
With triethylamine In dichloromethane at 30℃; for 4h; | 58% |
With triethylamine In dichloromethane at -30 - 20℃; for 7h; Inert atmosphere; | 20.2 g |
With triethylamine In dichloromethane at 0 - 20℃; | |
With triethylamine In dichloromethane at 20℃; Inert atmosphere; | 5.5 g |
(S)-1-Pyrrolidin-2-yl-methanol
4-[4-((2S)-2-hydroxymethylpyrrolidine-1-carbonyl)-2-methoxy-5-nitrophenoxy]butanoic acid methyl ester
Conditions | Yield |
---|---|
Stage #1: 4-[(3'-methoxycarbonylpropyl)oxy]-3-methoxy-2-nitrobenzoic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane at 20℃; Stage #2: (S)-1-Pyrrolidin-2-yl-methanol With triethylamine In dichloromethane at -30 - 20℃; | 100% |
(S)-1-Pyrrolidin-2-yl-methanol
3-[4-((2S)-2-hydroxymethylpyrrolidine-1-carbonyl)-2-methoxy-5-nitrophenoxy]propionic acid benzyl ester
Conditions | Yield |
---|---|
Stage #1: 4-(2-benzyloxycarbonylethoxy)-5-methoxy-2-nitrobenzoic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane at 20℃; Stage #2: (S)-1-Pyrrolidin-2-yl-methanol With triethylamine In dichloromethane at -30 - 20℃; | 100% |
N-tert-butyloxycarbonylpiperidin-4-one
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
Stage #1: N-tert-butyloxycarbonylpiperidin-4-one; (S)-1-Pyrrolidin-2-yl-methanol With sodium tris(acetoxy)borohydride; acetic acid In dichloromethane for 1h; Stage #2: With sodium hydrogencarbonate In dichloromethane; water Stage #3: With hydrogenchloride In 1,4-dioxane for 1h; | 100% |
2-chloro-4-(3-chloro-4-methoxybenzylamino)-5-ethoxycarbonylpyrimidine
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
at 20℃; | 100% |
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
In ethanol Reflux; | 100% |
(2-methylphenyl)(4-fluorophenyl)methanone
(S)-1-Pyrrolidin-2-yl-methanol
(S)-(4-(2-(hydroxymethyl)pyrrolidin-1-yl)phenyl)(o-tolyl)methanone
Conditions | Yield |
---|---|
at 175℃; for 0.166667h; Sealed tube; Microwave irradiation; | 100% |
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at -40℃; for 1h; | 100% |
(S)-1-Pyrrolidin-2-yl-methanol
((propane-1,3-diylbis(oxy))bis(5-methoxy-2-nitro-4,1-phenylene))bis(((S)-2-(hydroxymethyl)pyrrolidin-1-yl)methanone)
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at -40℃; for 1h; | 100% |
With triethylamine In dichloromethane at -40℃; for 1h; | 13.6 g |
1,3,5-trifluorobenzene
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With cesium fluoride In dimethyl sulfoxide at 80℃; for 48h; | 100% |
Methyl-2,2-dichlorhexanoat
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
In methanol at 25℃; for 24h; | 99% |
4,6-bis(bromomethyl)dibenzo[b,d]furan
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile | 99% |
(S)-1-Pyrrolidin-2-yl-methanol
benzeneacetic acid methyl ester
N-phenylacetyl-L-proplinol
Conditions | Yield |
---|---|
With N,N'-Mes2imidazol-2-ylidene In tetrahydrofuran at 23℃; for 4h; | 99% |
(Z)-4-(2'-bromo-3'-chloroprop-1'-enyl)-1,2-dimethoxybenzene
(S)-1-Pyrrolidin-2-yl-methanol
{(S)-1-[(Z)-2'-bromo-3'-(3'',4''-dimethoxyphenyl)prop-2'-enyl]pyrrolidin-2-yl}methanol
Conditions | Yield |
---|---|
With triethylamine In N,N-dimethyl-formamide at 70℃; for 16h; | 99% |
1-(2-(2-chloropyrimidin-4-yloxy)-5-fluorobenzyl)-3-(3-t-butyl-1-p-tolyl-1 H-pyrazol-5-yl)urea
(S)-1-Pyrrolidin-2-yl-methanol
(S)-1-(5-fluoro-2-(2-(2-(hydroxymethyl)pyrrolidin-1-yl)pyrimidin-4-yloxy)benzyl)-3-(3-t-butyl-1-p-tolyl-1H-pyrazol-5-yl)urea
Conditions | Yield |
---|---|
With sodium carbonate In ethanol at 60℃; for 2h; | 99% |
phenylacetylene
(S)-1-Pyrrolidin-2-yl-methanol
cyclohexanecarbaldehyde
Conditions | Yield |
---|---|
With Au/CeO2 In water at 100℃; for 6h; optical yield given as %de; | 99% |
4-methoxy-benzaldehyde
phenylacetylene
(S)-1-Pyrrolidin-2-yl-methanol
(2S)-1-(1-(4-methoxyphenyl)-3-phenylprop-2-yn-1-yl)-2-(hydroxymethyl)pyrrolidine
Conditions | Yield |
---|---|
With [Au(ppy)Cl2] In water at 40℃; for 24h; Inert atmosphere; diastereoselective reaction; | 99% |
With (N,N'-ethylenebis(salicylideniminato))gold(III) hexafluorophosphate In water at 40℃; for 24h; Darkness; Inert atmosphere; |
palladium diacetate
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
In dichloromethane under Ar; Pd acetate treated with ligand in CH2Cl2 at 20°C for 24h; evapd. to dryness; dissolved in min. CHCl3; filtered through cotton; filtrate evapd. to dryness; elem. anal.; | 99% |
(S)-1-Pyrrolidin-2-yl-methanol
Conditions | Yield |
---|---|
In dichloromethane under Ar; PdCl2 treated with ligand in CH2Cl2 at 20°C for 24 h; evapd. to dryness; dissolved in min. CHCl3; filtered through cotton; filtrate evapd. to dryness; elem. anal.; | 99% |
(S)-1-Pyrrolidin-2-yl-methanol
(S)-(1-(4-(o-tolylsulfonyl)phenyl)pyrrolidin-2-yl)methanol
Conditions | Yield |
---|---|
In dimethyl sulfoxide at 130℃; for 6h; | 99% |
In dimethyl sulfoxide at 130℃; for 6h; | 99% |
(S)-1-Pyrrolidin-2-yl-methanol
(5aS,10aS)-octahydrodipyrrolo[1,2-a:1',2'-d]pyrazine-5,10-dione
Conditions | Yield |
---|---|
With carbonylhydrido[6-(di-tert-butylphosphinomethylene)-2-(N,N-diethylaminomethyl)-1,6-dihydropyridine]ruthenium(II) In 1,4-dioxane at 135℃; for 19h; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
In toluene Inert atmosphere; Reflux; | 99% |
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