HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471038Generated: October 31, 2026
Chloroacetyl chloride → N-((1-Benzhydryl-3-hydroxyazetidin-3-yl)methyl)-2-chloroacetamide
https://huagongshe.com/reaction/471038
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(Aminomethyl)-1-(diphenylmethyl)azetidin-3-ol | HCID 20668533 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-((1-Benzhydryl-3-hydroxyazetidin-3-yl)methyl)-2-chloroacetamide | HCID 57988954 | — |
Reaction Steps
Chloroacetyl chloride (0.846 mL) was added dropwise over 30 minutes to a vigorously stirred mixture of 3-(aminomethyl)-1-benzhydrylazetidin-3-ol (example 33, step c) (2.1 g) in ethyl acetate (100 mL) and potassium carbonate (3.03 g) in water (100 mL) at 0° C. The mixture was stirred for a further 30 minutes at 0° C. and then extracted with ethyl acetate, the organic layer was dried over sodium sulphate, filtered and the solvent evaporated under reduced pressure to afford the subtitled compound. Yield 2.6 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08629271B2 |
|---|
| Source dataset | uspto-grants-2014_01 |
|---|
| ORD ID | ord-ea65ba7375d449bc9f06c4bca9c77645 |
|---|
| Source note | uspto-grants-2014_01 |
|---|