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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640191Generated: October 26, 2026

Ammonia → (4-(5-Methyl-furan-2-ylmethyl)-phenyl)-methanol

https://huagongshe.com/reaction/640191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantLithiumHCID 3028194—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant4-(Hydroxy-(5-methyl-furan-2-yl)-methyl)benzaldehydeHCID 59255336—
SolventTetrahydrofuranHCID 8028—
Product(4-(5-Methyl-furan-2-ylmethyl)-phenyl)-methanolHCID 59255234108.8%

Reaction Steps

To a mixture of lithium aluminumhydride (230 mg, 4.9 mmol) and tetrahydrofuran (15 mL) was added aluminum chloride (830 mg, 6.2 mmol) at 0° C., which was stirred for 30 minutes at room temperature. A mixture of 4-(hydroxy-(5-methyl-furan-2-yl)-methyl)-benzaldehyde (320 mg, 1.5 mmol) described in Manufacturing Example 46-1-1 and tetrahydrofuran (5 mL) was added dropwise into the reaction mixture at 0° C., and stirred for 2 hours at that temperature. A 28% aqueous ammonia solution was added dropwise into the reaction mixture at the same temperature to quench the excess reagent. The reaction mixture was cooled to room temperature, and filtered by being passed through a Celite bed. The filtrate was concentrated under a reduced pressure to obtain the title compound (330 mg) as a crude product. This compound was used in the following reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691882B2
Source datasetuspto-grants-2010_04
ORD IDord-f20aa5a2ea394992b7a5e9ed3eb94a10
Source noteuspto-grants-2010_04