HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177217Generated: November 1, 2026
Methyl 3,5-bis(methoxymethoxy)benzoate → 3,5-Bis(methoxymethoxy)benzylalcohol
https://huagongshe.com/reaction/1177217
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 3,5-bis(methoxymethoxy)benzoate | HCID 10106435 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,5-Bis(methoxymethoxy)benzylalcohol | HCID 10443751 | 92.7% |
Reaction Steps
To a solution of 3,5-bis-methoxymethoxy-benzoic acid methyl ester (220a) (350 g, 1.37 mol) in THF (1.8 L) was added portion wise LiAlH4 (62 g, 1.64 mol) at 0° C. The mixture was stirred at 0° C. for another 1 hr. TLC (EtOAc/petroleum ether=1/2) showed that the reaction was complete. The reaction was quenched with 2 N aqueous NaOH. The mixture was filtered through Celite. The filtrate was dried over Na2SO4 and concentrated to give the title compound (290 g, 76%) as a brown oil. 1H NMR (400 MHz, CDCl3): δ 6.70 (d, 2H), 6.64 (d, 1H), 5.22 (s, 4H), 4.61 (s, 2H), 3.46 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842713B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-93ee2dfd547343b0b20afee5ce5ba01f |
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| Source note | uspto-grants-2010_11 |
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