HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone Cyanohydrin → 5-[2-(Phenylmethoxy)ethyl]furan-2-propanenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone Cyanohydrin | HCID 6406 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | 2-(2-Hydroxyethyl)-5-[2-(phenylmethoxy)ethyl]furan | HCID 21875140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-[2-(Phenylmethoxy)ethyl]furan-2-propanenitrile | HCID 21875081 | 26% |
Reaction Steps
DEAD (1.285 mL, 8.17 mmol) was added to a stirred solution of Ph3P (2.14 g, 8.17 mmol) in 12 mL of dry THF at 0° C. The solution was stirred for 30 min at rt and compound 255E (670 mg, 2.72 mmol) was added. The reaction was stirred for 15 min and acetone cyanohydrin (0.745 mL, 8.17 mmol) was added at −15° C. The reaction was stirred for 30 min at −15° C., then at rt overnight. The mixture was then concentrated under reduced pressure. Purification by flash chromatography on silica gel eluting with 100% CH2Cl2 gave 180 mg (0.705 mmol, 26%) of compound 255F as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07470797B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-7b107dff56fc412f90c5a683497618d4 |
| Source note | uspto-grants-2008_12 |