HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethanolamine hydrochloride → 1-(2-iso-Propoxytetrahydro-3-furanyl)-1,2-ethanediol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethanolamine hydrochloride | HCID 518946 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl hydroxy-(2-isopropoxytetrahydro-3-furanyl)acetate | HCID 25242000 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(2-iso-Propoxytetrahydro-3-furanyl)-1,2-ethanediol | HCID 25242001 | — |
Reaction Steps
In a 2 L round bottom flask charged with 600 mL of ethanol and NaBH4 (12.55 g, 0.33 mol, 1.1 eq.) at 0° C., ethyl hydroxy-(2-isopropoxytetrahydro-3-furanyl)acetate (70 g, 0.3 mol, 1 eq.) dissolved in 400 mL of ethanol was added dropwise over 1 hour at 0° C. The mixture was allowed to warm up at room temperature and stirred for 19 hours. After cooling at 0° C., diethanolamine hydrochloride (46.7 g, 0.33 mol, 1.1 eq.) dissolved in 100 mL of water was added over 10 min. and stirred for 8 hours. The solvent was evaporated under reduced pressure to afford a clear yellow solid. After dilution with 300 mL of ethylacetate, the heterogeneous mixture was filtered over dicalite. The mixture was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08153829B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-b018d2d89a6b4f599925463454d95fb8 |
| Source note | uspto-grants-2012_04 |