HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 31215Generated: October 30, 2026
Water → 2-[2,5-Bis(benzyloxy)phenoxy]-1-phenylethanol
https://huagongshe.com/reaction/31215
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-[2,5-Bis(benzyloxy)phenoxy]-1-phenylethanone | HCID 17978482 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[2,5-Bis(benzyloxy)phenoxy]-1-phenylethanol | HCID 17978469 | — |
Reaction Steps
To the solution of 2-[2,5-bis(benzyloxy)phenoxy]-1-phenylethanone (0.14 g) in methanol (0.5 ml) and tetrahydrofuran (1.9 ml) was added at the 0° C. temperature sodium borohydride (6.5 mg). The reaction was stirred 15 minutes at 0° C. and 2 hrs at 22° C. temperature. After adding water (5 ml) methanol and tetrahydrofuran were evaporated off. After the residue was stirred at 22° C. 0.5 hr the product was filtered, washed with cold water and dried under reduced pressure. Yield is 0.09 g. 1H NMR (DMSO-d4) δ=4.05 (m, 2H), 4.91 (m, 1H), 4.95 (s, 2H), 5.01 (s, 2H), 5.59 (d, J=4.7 Hz, 1H), 6.47 (dd, J=2.8, 8.8 Hz, 1H), 6.68 (d, J=2.8 Hz, 1H), 6.89 (d, J=8.8 Hz, 1H), 7.24-7.45 (m, 15H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07425568B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-69d11df7168f4cb186f8d046666e8b1e |
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| Source note | uspto-grants-2008_09 |
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