6-(Hydroxymethyl)morpholin-3-one

Base Information

• Chemical Name: 6-(Hydroxymethyl)morpholin-3-one
• CAS No.: 929019-95-4
• Molecular Formula: C5H9NO3
• Molecular Weight: 131.131
• Hs Code.: 2934999090
• DSSTox Substance ID: DTXSID50694973
• Mol file: 929019-95-4.mol

Synonyms:6-(Hydroxymethyl)morpholin-3-one;929019-95-4;SCHEMBL617665;DTXSID50694973;DMELBDGPDOJCTC-UHFFFAOYSA-N;AMY21703;AB7325;MFCD11044016;AKOS006308885;SB45445;SB45474;AS-44835;EN300-95732;A859934;F8887-6661

Chemical Property of 6-(Hydroxymethyl)morpholin-3-one

Chemical Property:

• Boiling Point: 397.1±27.0 °C(Predicted)
• PKA: 13.98±0.40(Predicted)
• PSA: 62.05000
• Density: 1 +-.0.06 g/cm3(Predicted)
• LogP: -1.23040
• Storage Temp.: Sealed in dry,Room Temperature
• XLogP3: -1.4
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 131.058243149
• Heavy Atom Count: 9
• Complexity: 115

Purity/Quality:

97% ^*data from raw suppliers

6-(Hydroxymethyl)morpholin-3-one ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1C(OCC(=O)N1)CO

Technology Process of 6-(Hydroxymethyl)morpholin-3-one

There total 1 articles about 6-(Hydroxymethyl)morpholin-3-one 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:

N-(2,3-dihydroxypropyl)-chloroacetamide (71064-34-1) → 6-(hydroxymethyl)morpholin-3-one (929019-95-4)

Guidance literature:

With potassium tert-butylate; In tert-Amyl alcohol; for 1h; Inert atmosphere;

Reference yield:

6-(hydroxymethyl)morpholin-3-one (929019-95-4) + p-toluenesulfonyl chloride (98-59-9) → (5-oxomorpholin-2-yl)methyl 4-methylbenzenesulfonate (1005474-84-9)

Guidance literature:

With triethylamine; In dichloromethane; at 0 - 20 ℃;

Reference yield:

6-(hydroxymethyl)morpholin-3-one (929019-95-4) → tert-butyl ((R)-1-(naphthalen-1-yl)ethyl)((5-oxo-4-phenylmorpholin-2-yl) methyl)carbamate (1398397-11-9)

Guidance literature:

Multi-step reaction with 4 steps

1: triethylamine / dichloromethane / 0 - 20 °C

2: 2 h / 120 °C / Microwave irradiation

3: triethylamine / dichloromethane / 0 - 20 °C

4: N,N-dimethyl-ethanamine / copper(l) iodide / 1,4-dioxane / 110 °C

With N,N-dimethyl-ethanamine; triethylamine; copper(l) iodide; In 1,4-dioxane; dichloromethane; 4: Buchwald-Hartwig Coupling;

upstream raw materials:

N-(2,3-dihydroxypropyl)-chloroacetamide

Downstream raw materials:

(5-oxomorpholin-2-yl)methyl 4-methylbenzenesulfonate

tert-butyl ((R)-1-(naphthalen-1-yl)ethyl)((5-oxo-4-phenylmorpholin-2-yl) methyl)carbamate

6-((((R)-1-(naphthalen-1-yl)ethyl)amino)methyl)-4-phenylmorpholin-3-one

6-((((R)-1-(naphthalen-1-yl)ethyl)amino)methyl)-4-phenylmorpholin-3-one

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