HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → tert-butyl 4-[(1S)-1-hydroxyethyl]benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Diethanolamine | HCID 8113 | — |
| Reactant | Chlorobis((1R,2S,3R,5R)-2,6,6-trimethylbicyclo[3.1.1]heptan-3-yl)borane | HCID 11131038 | — |
| Reactant | tert-Butyl 4-acetylbenzoate | HCID 13844704 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | tert-butyl 4-[(1S)-1-hydroxyethyl]benzoate | HCID 70815081 | 103.3% |
Reaction Steps
To tert-butyl 4-acetylbenzoate (3.33 g) in a tetrahydrofuran (23 ml) solution, (−)-B-chlorodiisopinocampheylborane in a 65% hexane solution (11.2 ml) was added dropwise under ice cooling, then the mixture was stirred at that temperature for 1.5 hours. The reaction solution was concentrated, and the residue was diluted by diethyl ether. To the thus solution obtained, diethanolamine (4.3 ml) was added under ice cooling, and the mixture was stirred at room temperature for 2 hours. The precipitates were removed by filtration, and the filtrate was concentrated. The residue was purified by flash column chromatography (silica gel, hexane/ethyl acetate=9/1 to 4/1) to obtain the title compound (3.47 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846660B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-1a363a750112412691c011c2365672b9 |
| Source note | uspto-grants-2014_09 |