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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7872Generated: October 26, 2026

Hydrochloric Acid → (2SR,9aSR)-2-ALLYL-9a-BUTYL-7-HYDROXY-4-METHYL-1,2,9,9a-TETRAHYDRO-3H-FLUOREN-3-ONE

https://huagongshe.com/reaction/7872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant(2SR,9aSR)-2-allyl-9a-butyl-7-methoxymethoxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-oneHCID 67401390—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(2SR,9aSR)-2-ALLYL-9a-BUTYL-7-HYDROXY-4-METHYL-1,2,9,9a-TETRAHYDRO-3H-FLUOREN-3-ONEHCID 9922724—

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of (2SR,9aSR)-2-allyl-9a-butyl-7-methoxymethoxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one (5 mg, 0.015 mmol) in THF (0.5 mL) was treated with 6N HCl (0.5 mL) and the resulting solution was heated at 50° C. overnight. The mixture was diluted with EtOAc (30 mL), washed with 5% NaHCO3 and brine, dried over MgSO4, filtered, and evaporated under vacuum to a yellow oil. The crude product was purified by PLC on a 0.025×20×20 cm silica gel GF plate using 2:1 hexanes-EtOAc as developing solvent. The UV visible band at Rf 0.43-0.57 afforded (2SR,9aSR)-2-allyl-9a-butyl-7-hydroxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one as a gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087599B2
Source datasetuspto-grants-2006_08
ORD IDord-cf2f58d1d9b2468d8835b967eb71e56a
Source noteuspto-grants-2006_08