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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 6-benzyloxy-5-tert-butyl-4'-methyl-3-biphenylcarboxylate | HCID 12084817 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Benzyloxy-5-tert-butyl-4'-methyl-3-biphenylcarbaldehyde | HCID 12084818 | 85% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07468457B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-ade757147fc0433d88be1d0a13bf61c9 |
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| Source note | uspto-grants-2008_12 |
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