HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537608Generated: October 29, 2026
Hydrochloric Acid → 2-Methoxy-4-(2',2',2'-tris(octadecyloxymethyl)ethoxy)benzyl alcohol
https://huagongshe.com/reaction/537608
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Methoxy-4-(2',2',2'-tris(octadecyloxymethyl)ethoxy)benzaldehyde | HCID 86654890 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Methoxy-4-(2',2',2'-tris(octadecyloxymethyl)ethoxy)benzyl alcohol | HCID 53258810 | — |
Reaction Steps
2-Methoxy-4-(2′,2′,2′-tris(octadecyloxymethyl)ethoxy)benzaldehyde (288 mg, 280 μmol) was dissolved in THF (3 ml), methanol (0.3 ml) and sodium borohydride (31.8 mg, 841 μmol) were added, and the mixture was stirred at 60° C. for 2 hr. The reaction mixture was cooled to room temperature, 1N hydrochloric acid (5 ml) and chloroform (5 ml) were added, and the mixture was stirred. The aqueous layer was removed, and the organic layer was further washed twice with purified water (5 ml). The organic layer was evaporated under reduced pressure, and the residue was azeotropically distilled with acetonitrile and dried in vacuo to give 2-methoxy-4-(2′,2′,2′-tris(octadecyloxymethyl)ethoxy)benzyl alcohol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859732B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-9ffa79220a794fe9ae4cda6444b03c32 |
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| Source note | uspto-grants-2014_10 |
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