C₅H₁₁NO₂*ClH

Base Information

Chemical Name:C₅H₁₁NO₂*ClH
CAS No.:1018987-47-7
Molecular Formula:C₅H₁₁NO₂*ClH
Molecular Weight:153.609
Hs Code.:

C<sub>5</sub>H<sub>11</sub>NO<sub>2</sub>*ClH

Synonyms:

Suppliers and Price of C₅H₁₁NO₂*ClH

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

American Custom Chemicals Corporation
(3S,5R)-5-(HYDROXYMETHYL)PYRROLIDIN-3-OL HYDROCHLORIDE 95.00%
5MG
$ 452.18

Ambeed
(3S,5R)-5-(HYdroxymethyl)pyrrolidin-3-olhydrochloride 98%
5g
$ 662.00

Ambeed
(3S,5R)-5-(HYdroxymethyl)pyrrolidin-3-olhydrochloride 98%
1g
$ 189.00

Ambeed
(3S,5R)-5-(HYdroxymethyl)pyrrolidin-3-olhydrochloride 98%
250mg
$ 73.00

Total 6 raw suppliers

Chemical Property of C₅H₁₁NO₂*ClH

Chemical Property:

Purity/Quality:

99%, ^*data from raw suppliers

(3S,5R)-5-(HYDROXYMETHYL)PYRROLIDIN-3-OL HYDROCHLORIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₅H₁₁NO₂*ClH

There total 4 articles about C₅H₁₁NO₂*ClH 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: 90.0%

: 1448706-36-2
(2R,4S)-2-hydroxymethyl-4-hydroxy-N-(carbobenzyloxy)pyrrolidine

: 1018987-47-7,478922-47-3
C₅H₁₁NO₂*ClH

Guidance literature:: (2R,4S)-2-hydroxymethyl-4-hydroxy-N-(carbobenzyloxy)pyrrolidine; With 20% palladium hydroxide-activated charcoal; hydrogen; In ethanol; under 760.051 Torr;

With hydrogenchloride; In methanol;
DOI:10.1016/j.bmcl.2013.06.030

Reference yield:

: 130930-25-5
(R,R)-4-hydroxy-1-(benzyloxycarbonyl)pyrrolidine-2-carboxylic acid

: 1018987-47-7,478922-47-3
C₅H₁₁NO₂*ClH

Guidance literature:: Multi-step reaction with 4 steps

1: methanol

2: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 0.05 h

3: lithium borohydride / tetrahydrofuran / 23 °C

4: hydrogen; 20% palladium hydroxide-activated charcoal / ethanol / 760.05 Torr

With lithium borohydride; di-isopropyl azodicarboxylate; 20% palladium hydroxide-activated charcoal; hydrogen; triphenylphosphine; In tetrahydrofuran; methanol; ethanol; 2: |Mitsunobu Displacement;
DOI:10.1016/j.bmcl.2013.06.030

Reference yield:

: 155075-23-3
(2R,4R)-1-benzyl 2-methyl 4-hydroxypyrrolidine-1,2-dicarboxylate

: 1018987-47-7,478922-47-3
C₅H₁₁NO₂*ClH

Guidance literature:: Multi-step reaction with 3 steps

1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 0.05 h

2: lithium borohydride / tetrahydrofuran / 23 °C

3: hydrogen; 20% palladium hydroxide-activated charcoal / ethanol / 760.05 Torr

With lithium borohydride; di-isopropyl azodicarboxylate; 20% palladium hydroxide-activated charcoal; hydrogen; triphenylphosphine; In tetrahydrofuran; ethanol; 1: |Mitsunobu Displacement;
DOI:10.1016/j.bmcl.2013.06.030