HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(2-(3-Methoxyphenyl)ethyl)phenol → 4-t-Butoxycarbonyl-2-{2-[2-(3-methoxyphenyl)ethyl]phenoxymethyl}morpholine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(2-(3-Methoxyphenyl)ethyl)phenol | HCID 10585448 | — |
| Reactant | N-BOC-2-(tosyloxymethyl)morpholine | HCID 19423893 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 4-t-Butoxycarbonyl-2-{2-[2-(3-methoxyphenyl)ethyl]phenoxymethyl}morpholine | HCID 10717379 | 99.9% |
Reaction Steps
Following a procedure similar to that described in Example 40, 1.00 g of 2-[2-(3-methoxyphenyl)ethyl]phenol (prepared as described in Preparation 20), 1.63 g of 4-t-butoxycarbonyl-2-(p-toluenesulfonyloxymethyl)morpholine and 0.490 g of potassium t-butoxide were reacted in 20 ml of dimethylacetamide. The mixture was then worked up as described in Example 40, and the crude product thus obtained was purified by column chromatography through silica gel, using a 4:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 1.87 g (yield 94.5%) of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05556864 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-5d14d6df21654277b477188a471a393e |
| Source note | uspto-grants-1996_09 |