HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 3-[(2-Methoxyethoxy)carbonylamino]benzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-Methoxyethyl chloroformate | HCID 69400 | — |
| Reactant | 3-Aminobenzyl alcohol | HCID 80293 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-[(2-Methoxyethoxy)carbonylamino]benzyl alcohol | HCID 67347770 | — |
Reaction Steps
To a solution of 15.0 g of 3-aminobenzyl alcohol in 120 ml of tetrahydrofuran was added dropwise a solution of 18 ml of 2-methoxyethyl chloroformate in 70 ml of tetrahydrofuran under ice-cooling. After stirred for 30 minutes under ice-cooling and then at room temperature for 30 minutes, additional 2 ml of 2-methoxyethyl chloroformate was added, and the mixture was stirred at room temperature for 1 hour. After ethyl acetate was added, the mixture was washed successively with an aqueous saturated sodium bicarbonate solution and then an aqueous saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and then concentrated to obtain 30.2 g of 3-[(2-methoxyethoxy)carbonylamino]benzyl alcohol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07691883B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-fade4e6a07bf4952974b2573a70727ec |
| Source note | uspto-grants-2010_04 |