HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929490Generated: October 30, 2026
4-Methoxybenzyl bromide → HCID 58155181, compound
https://huagongshe.com/reaction/1929490
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methoxybenzyl bromide | HCID 165021 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 66931638 | HCID 66931638 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58155181 | HCID 58155181 | — |
Reaction Steps
A solution of (R)-5-(3-amino-phenyl)-4-(4-methoxy-benzyl)-5-methyl-morpholin-3-one (1.0 g, 3.7 mmol) in N,N-dimethylformamide was added within 5 minutes at 0° C. to a solution of potassium tert-butanolate (0.636 g, 5.7 mmol). After stirring at 0° C. for 30 minutes the light yellow solution was cooled to −4° C. and treated with a solution of 4-methoxybenzylbromide (1.12 g, 5.6 mmol) in N,N-dimethylformamide (4 ml). The reaction mixture was left to warm to room temperature, then the solvent was evaporated at reduced pressure, and the residue treated with saturated ammonium chloride solution (50 ml) and ethyl acetate (100 ml). The organic layer was separated, washed with brine (50 ml), dried over sodium sulfate, and evaporated at reduced pressure. The crude product was purified by chromatography on silica gel using a gradient of heptane and ethyl acetate=100/0 to 50/50 as the eluent. The (R)-5-(3-bromo-phenyl)-4-(4-methoxy-benzyl)-5-methyl-morpholin-3-one was obtained as colorless oil (1.19 g, 83% of theory). Mass (calculated) C19H20BrNO3 [390.275]; (found) [M+H]+=390, [M+2-H]+=392.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08188079B2 |
|---|
| Source dataset | uspto-grants-2012_05 |
|---|
| ORD ID | ord-df916bd456fe46e29356ad28103a1908 |
|---|
| Source note | uspto-grants-2012_05 |
|---|