HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790480Generated: November 2, 2026
6-Methoxy-1-Indanone → HCID 12374669, compound
https://huagongshe.com/reaction/1790480
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 6-Methoxy-1-Indanone | HCID 334036 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 12374669 | HCID 12374669 | 100.7% |
Reaction Steps
6-Methoxyindan-1-one (5.0 g) was dissolved in methanol (50 ml). Next, sodium tetrahydroborate (1.41 g) was added thereto at 0° C., and the resultant mixture was reacted at room temperature for 5 hr. The reaction solution was concentrated under reduced pressure and the residue was partitioned between ethyl acetate and water. The ethyl acetate layer was washed with water, dried and concentrated under reduced pressure to give 6-methoxyindan-1-ol (5.1 g) as an oil. This alcohol was not purified but reacted as such with thionyl chloride (4.5 ml) in ether at room temperature for 6 hr. The reaction solution was poured into ice water and extracted with ether. The ether layer was washed with water, dried and concentrated under reduced pressure to give the title compound (2.76 g). (251-2) 1-(4-Acetylpiperazin-1-yl)-6-methoxyindan
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07071201B2 |
|---|
| Source dataset | uspto-grants-2006_07 |
|---|
| ORD ID | ord-5560cc829e98483ca2ad1691a83b6d91 |
|---|
| Source note | uspto-grants-2006_07 |
|---|