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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246623Generated: October 30, 2026

Sodium borohydride → HCID 57419668, compound

https://huagongshe.com/reaction/1246623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57419667HCID 57419667—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57419668HCID 57419668—

Reaction Conditions

Temperature45 °C

Reaction Steps

The allyl ether from stage (ii) (800 mg, 4.16 mmol) was dissolved in THF (10 mL) and treated with palladium tetrakis(triphenylphosphine) (481 mg, 0.42 mmol) followed by sodium borohydride (944 mg, 25 mmol). The mixture was then heated to 45° C. and stirred at this temperature for 15 h. After cooling to room temperature the THF was evaporated and the residue partitioned between 2M NaOH solution (25 mL) and diethyl ether (25 mL). The aqueous layer was separated and the organic layer re-extracted with 2M NaOH solution (25 mL). The combined aqueous layers were neutralised to pH 7–8 with concentrated hydrochloric acid and extracted with EtOAc (2×25 mL). The combined organic extracts were dried (MgSO4) and evaporated to a clear oil of the title phenol which solidified upon standing (540 mg, 85%); 4.14 (2H, s), 4.17 (2H, s), 6.63–6.68 (2H, m), 7.04 (1H, d)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129234B2
Source datasetuspto-grants-2006_10
ORD IDord-7af69bb09f9d4269a6e2273d2783ddb6
Source noteuspto-grants-2006_10