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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351821Generated: October 29, 2026

Sodium Hydroxide → Piperonyl alcohol

https://huagongshe.com/reaction/351821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 1,3-benzodioxole-5-carboxylateHCID 81391—
ReactantAluminium lithium hydrideHCID 21226445—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductPiperonyl alcoholHCID 1032294.5%

Reaction Steps

To a mixture of 0.99 g (26.16 mmol) of LiAlH4 and 80 mL of Et2O, 2.54 g (13.08 mmol) of ethyl 3,4-(methylenedioxy)benzoate (obtained in the preceding section) dissolved in 160 mL of Et2O was added under argon, and the mixture was stirred overnight at room temperature. A mixture of 1.62 mL of H2O and 3.41 mL of THF, followed by 1.62 mL of 15% NaOH and then 4.43 mL of H2O were added dropwise. The resulting mixture was filtered, washed with Et2O and EtOAc, and the solvent was evaporated. The residue was partitioned between H2O and EtOAc, the layers were separated, the aqueous phase was extracted with EtOAc and the combined organic phases were dried over MgSO4 and concentrated, yielding 1.88 g of the desired product (94% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743816B2
Source datasetuspto-grants-2004_06
ORD IDord-5b8d4825516c4a4c904b4cdf4816d49f
Source noteuspto-grants-2004_06