HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899572Generated: October 30, 2026
Sodium borohydride → HCID 16738000, compound
https://huagongshe.com/reaction/899572
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-phenoxynaphthaldehyde | HCID 10824435 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 16738000 | HCID 16738000 | 99.9% |
Reaction Steps
To a solution of 134 (0.28 g, 1.12 mmol) in ethanol (20 mL) was added sodium borohydride (0.042 g, 1.12 mmol). After stirring at room temperature for 15 min, the reaction was quenched with water and extracted with ethyl ether. The organic layer was washed with brine, dried over magnesium sulfate, filtered, and concentrated under reduced pressure to give the crude product. The crude mixture was purified via flash SiO2 chromatography (ethyl acetate/hexanes (25%/75%) to give 135 (0.28 g, 95% yield): 1H-NMR (400 MHz, chloroform-d) δ 8.29 (d, J=8.3 Hz, 1H), 8.17 (d, J=8.3 Hz, 1H), 7.61 (m, 1H), 7.53 (m, 1H), 7.41 (d, J=7.8 Hz, 1H), 7.35 (t, J=7.8 Hz, 2H), 7.13 (t, J=7.3 Hz, 1H), 7.05 (dd, J=8.6, 1.2 Hz, 2H), 6.88 (d, J=7.8 Hz, 1H), 5.12 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07355079B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-eb146e2d79494277aeb1f200d13a9674 |
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| Source note | uspto-grants-2008_04 |
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