HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethanolamine → 2-Chloro-1-phenylethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethanolamine | HCID 8113 | — |
| Reactant | 2-Chloroacetophenone | HCID 10757 | — |
| Reactant | Chlorobis(2,6,6-trimethylbicyclo(3.1.1)heptan-3-yl)borane | HCID 13515837 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Chloro-1-phenylethanol | HCID 92898 | — |
Reaction Steps
2-Chloroacetophenone (6.25 g., 40.4 mmol) was treated with (+) DIP-chloride (18 g., 56.1 mmol) in anhydrous THF (40 mL) at dry-ice bath temperature and left overnight. The temperature was raised to room temperature and THF was removed in vacuo. The residue was dissolved in ether (210 mL). The diethanolamine (9 g., 8 5.6 mmol) was added and the mixture stirred at room temperature for 5 hrs. The separated solid was filtered and the filtered cake was washed with ether (150 mL). The combined filtrates were evaporated to dryness to give 15.53 g. of crude product. This was purified by silica gel column chromatography using 1% ether and petroleum ether 4.32 g (68%) of the desired product as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07166625B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-fd9955d341c746b2b247ccd576913ea0 |
| Source note | uspto-grants-2007_01 |