HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573966Generated: November 1, 2026
Hydrochloric Acid → 2,3,4-Tris(octadecyloxy)benzhydryl alcohol
https://huagongshe.com/reaction/573966
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2,3,4-Trioctadecanoxybenzophenone | HCID 59510351 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2,3,4-Tris(octadecyloxy)benzhydryl alcohol | HCID 46936047 | 99% |
Reaction Steps
2,3,4-Tris(octadecyloxy)benzophenone (3.00 g, 3.04 mmol) was dissolved in a mixed solvent of chloroform (30 mL) and methanol (10 mL), sodium borohydride (360 mg, 9.51 mmol) was added, and the mixture was stirred at 45° C. for 2 hr. After completion of the reaction, 0.1 mol/L aqueous hydrochloric acid was added dropwise to decompose unreacted sodium borohydride and the mixture was washed with 1.0 mol/L aqueous hydrochloric acid. The organic layer was dried over sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. Methanol was added to the concentrated solution, and the precipitated solid was collected by filtration and dried under reduced pressure to give the title compound (2.98 g, 99.0%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029528B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-904ad277d0ce49d382b1dcbb8dc0acc7 |
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| Source note | uspto-grants-2015_05 |
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