HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975923Generated: October 31, 2026
Sodium borohydride → HCID 19968570, compound
https://huagongshe.com/reaction/975923
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 19968564 | HCID 19968564 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 19968570 | HCID 19968570 | 100.5% |
Reaction Steps
To a solution of 6-methoxy-5-nitro-3,4 -dihydronaphthalene-1-carbonitrile (0.41 g, 1.8 mmol) in 10 ml of EtOH was added NaBH4 (0.20 g, 5.3 mmol) and the resulting reaction mixture was stirred for 30 min at 25° C. The solvent was removed in vacuo to yield an oily residue which was dissolved in EtOAc and washed with brine. The organic layer was dried over Na2SO4 and concentrated in vacuo to yield the desired product as a colorless oil (0.42 g, >95%) which was subjected to a following reaction without purification. 1H NMR (300 MHz, CDCl3):δ 1.86 (m, 2H), 2.04 (m, 2H), 2.62 (q, 2H, J=6.3 Hz), 3.83 (s, 3H), 4.17 (t, 1H, J=6.3 Hz), 7.10 (d, 1H, J=8.9 Hz), 7.45 (d, 2H, J=8.9 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05610174 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-3f71952513f14e19b4f7ca65fc9b0349 |
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| Source note | uspto-grants-1997_03 |
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