HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108655Generated: October 30, 2026
HCID 86603464, compound → HCID 86603465, compound
https://huagongshe.com/reaction/2108655
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 86603464 | HCID 86603464 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl acetate acetate | HCID 22609514 | — |
| Product | HCID 86603465 | HCID 86603465 | 100% |
Reaction Steps
A mixture of 2,4-dimethyl-6-hydroxy-3-(4′-methoxymethoxy-3′-iso-propylbenzyl)benzyl alcohol ((0.20 g, 0.58 mmol) and Pd—C (0.08 g, 10%) in ethyl acetate-acetic acid (3.5 mL, 95:5) was stirred at room temperature under a H2 atmosphere for 6 h. The reaction mixture was filtered through a Celite plug and the solvent was removed under reduced pressure to afford 4-(4′-methoxymethoxy-3′-iso-propylbenzyl)-2,3,5-trimethylphenol (0.19 g, 100%) as colorless oil: 1H NMR (300 MHz, CD3OD): δ 6.94 (m, 1H), 6.91 (d, J=13.2 Hz, 1 H), 6.68 (dd, J=13.2, 2.4 Hz, 1 H), 6.55 (s, 1 H), 5.17 (s, 2 H), 3.95 (s, 2 H), 3.47 (s, 3 H), 3.30 (m, 1 H), 2.19 (s, 3 H), 2.16 (s, 3 H), 2.11 (s, 3 H), 1.17 (d, J=10.8 Hz, 6 H); TLC conditions: Uniplate silica gel, 250 microns; Mobile phase=acetone-hexanes (3:7); Rf=0.60.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07514419B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-c8404f44efff494e88ef455fb61972a9 |
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| Source note | uspto-grants-2009_04 |
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