Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | HCID 67032756 | HCID 67032756 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67032412 | HCID 67032412 | 102.8% |
Reaction Steps
Acetyl chloride (1.35 mL, 8.9 mmol) was added to ethanol (60 mL). The resulting solution was added to 2-[4-(2,6-dichloro-benzyloxy)-phenyl]-morpholine-4-carboxylic acid tert-butyl ester (1.54 g; 3.4 mmol), at RT. The resulting mixture was stirred at 60° C. for 3 hours, and subsequently, at RT for three days. The resulting suspension was concentrated in vacuo, and treated with iPr2O. The formed precipitate was collected by filtration and dried in vacuo to afford 2-[4-(2,6-dichloro-benzyloxy)-phenyl]-morpholine hydrochloride (1.31 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09045441B2 |
|---|
| Source dataset | uspto-grants-2015_06 |
|---|
| ORD ID | ord-f905850a0be54a76969441e6e4a1711a |
|---|
| Source note | uspto-grants-2015_06 |
|---|