HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7832Generated: October 29, 2026
Acetic Acid → HCID 21990921, compound
https://huagongshe.com/reaction/7832
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 2-Butyl-5-methoxy-2-(3-oxo-butyl)-1-indanone | HCID 21990854 | — |
| Product | HCID 21990921 | HCID 21990921 | — |
Reaction Steps
The solution from step 2 was treated with pyrrolidine (6.9 mL, 82 mmol) and acetic acid (4.7 mL, 82 mmol), placed under a nitrogen atmosphere, and stirred with heating in a 60° C. bath for 22 hours. After cooling to room temperature, the reaction mixture was partitioned between EtOAc (500 mL) and water (500 mL). The EtOAc phase was washed with 0.8N HCl (500 mL), water (500 mL), 5% NaHCO3 (500 mL), and brine (200 mL), dried with MgSO4, filtered, and evaporated under vacuum to a brown oil (22.8 g). This material was purified by column chromatography on EM silica gel 60 (230-400 mesh, 684 g), using 5% EtOAc in CH2Cl2 as eluting solvent, to afford 9a-butyl-7-methoxy-1,2,9,9a-tetrahydro-3H-fluoren-3-one (11.2 g) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07087599B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-6eb19596dc4f425b98b352cad4d4b671 |
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| Source note | uspto-grants-2006_08 |
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