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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377199Generated: October 31, 2026

Water → 6-Benzyloxy-5-tert-butyl-4'-methyl-3-biphenylcarbaldehyde

https://huagongshe.com/reaction/2377199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 6-benzyloxy-5-tert-butyl-4'-methyl-3-biphenylcarboxylateHCID 12084817—
ReactantAluminium lithium hydrideHCID 21226445—
CatalystHCID 178418406HCID 178418406—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product6-Benzyloxy-5-tert-butyl-4'-methyl-3-biphenylcarbaldehydeHCID 1208481885%

Reaction Conditions

Temperature0 °C

Reaction Steps

1 g (2.6 mmol) of methyl 6-benzyloxy-5-tert-butyl-4′-methyl-3-biphenylcarboxylate is dissolved in 40 mL of anhydrous ethyl ether, and the medium is cooled to 0° C. 130 mg (3.3 mmol) of lithium aluminum hydride are added and the reaction medium is stirred for 1 hour. The reaction is hydrolysed by sequential addition of 130 μL of water, 130 μL of 15% sodium hydroxide solution and 400 μL of water. The reaction medium is filtered and the filtrate is concentrated under reduced pressure. The residue obtained is dissolved in 30 mL of dichloromethane, and 2 g (23 mmol) of manganese dioxide are added. The medium is refluxed for 5 hours, and filtered through Celite. A yellow oil is obtained (m=780 mg; yield=85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468457B2
Source datasetuspto-grants-2008_12
ORD IDord-ade757147fc0433d88be1d0a13bf61c9
Source noteuspto-grants-2008_12