HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Chloro-1,3-dihydro-2-benzofuran-1-one → 5-Chloro-1,3-dihydroisobenzofuran-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Chloro-1,3-dihydro-2-benzofuran-1-one | HCID 241737 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Chloro-1,3-dihydroisobenzofuran-1-ol | HCID 69310156 | — |
Reaction Steps
To a solution of 5-chlorophthalide (3.64 g, 21.6 mmol) in dichloromethane (100 mL) at −78° C. was added di-isobutylaluminium hydride (1M in toluene) (23.8 mL, 23.8 mmol) dropwise. After 1 h the reaction mixture was quenched with a saturated solution of sodium tartrate (250 mL), allowed to warm to room temperature and stirred for 1 h. The layers were separated and the aqueous layer extracted with dichloromethane. The combined organic layers were dried (MgSO4), filtered and concentrated in vacuo to yield the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07335660B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-90efd2f51e8b47b0acab76f70b34e200 |
| Source note | uspto-grants-2008_02 |