Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | 3-Amino-1,2-propanediol | HCID 73561 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 13233120 | HCID 13233120 | 64.9% |
Reaction Steps
3-Amino-1,2-propanediol (16.8 g, 184 mmol) was dissolved in MeOH (90 mL) at RT and the solution was diluted with ACN (acetonitrile) (550 mL) TEA (30.5 mL, 219 mmol) was added and the reaction mixture was cooled to −10° C. Chloroacetyl chloride (22.2 g, 15.6 mL, 197 mmol) was added dropwise at −10° C. for 2 h under nitrogen atmosphere and further maintained at −10° C. for 1 h and the reaction mixture was allowed to RT and stirred overnight (15 h). The solvents were removed under vacuo. The residue was purified by flash column chromatography (normal phase, gradient 1 percent to 20 percent MeOH in EtOAc) to afford the title compound (20 g) as a colorless oil m/z 168.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09382216B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-e1d43fadf6f24289bfdbb89a07dcc3b2 |
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| Source note | uspto-grants-2016_07 |
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