HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → Ethyl 4-(alpha-hydroxybenzyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Ethyl 4-iodobenzoate | HCID 142891 | — |
| Reactant | HCID 178461729 | HCID 178461729 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | Ethyl 4-(alpha-hydroxybenzyl)benzoate | HCID 10244131 | 90% |
Reaction Steps
A solution of 552 mg (2 mmol) of ethyl 4-iodobenzoate in 20 ml of THF was cooled to −40° C. and 1.06 mmol of diisopropylmagnesium in methyl tert-butyl ether were added. After 1 h at −40° C. 233 mg (2.2 mmol) of benzaldehyde were added. After 3 h, the reaction mixture was hydrolyzed and the org. phase was concentrated. Chromatography of the crude product with 4/1 pentane/ether afforded 460 mg (90%) of the alcohol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06899830B1 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-8a4168880ee44c6cb5d5966673868e61 |
| Source note | uspto-grants-2005_05 |