HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710236Generated: October 29, 2026
N-Methoxy-N-methylacetamide → tert-Butyl 2-(4-acetylphenyl)morpholine-4-carboxylate
https://huagongshe.com/reaction/710236
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methoxy-N-methylacetamide | HCID 537505 | — |
| Reactant | Tert-butyl 2-(4-bromophenyl)morpholine-4-carboxylate | HCID 58097878 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butyl 2-(4-acetylphenyl)morpholine-4-carboxylate | HCID 89689432 | — |
Reaction Steps
tert-Butyl 2-(4-bromophenyl)morpholine-4-carboxylate (750 mg, 2.19 mmol, CAS 1131220-82-0) in THF (6 ml) was cooled to −78° C., treated dropwise with n-butyllithium (2.05 ml, 3.29 mmol, 1.6 M solution in hexane) and stirred 1 h at −78° C. N-Methoxy-N-methylacetamide (226 mg, 2.19 mmol) was added and the mixture was stirred for 1 h at −78° C., and then allowed to warm up to −5° C. The reaction mixture was quenched by addition of saturated ammonium chloride solution (4 ml) and water (4 ml) and the resulting mixture was partitioned between water and ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09181230B2 |
|---|
| Source dataset | uspto-grants-2015_11 |
|---|
| ORD ID | ord-e8f36dce21474d75927ad3cec26f6f15 |
|---|
| Source note | uspto-grants-2015_11 |
|---|