HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397038Generated: October 30, 2026
Sodium borohydride → HCID 18172410, compound
https://huagongshe.com/reaction/397038
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 18172446 | HCID 18172446 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 18172410 | HCID 18172410 | 99.4% |
Reaction Steps
Sodium borohydride (0.34 g, 0.89 mmol) was added in small portions to a solution of 1-(4-benzyloxyphenyl)-3,4-dihydroisoquinoline (0.139 g, 0.44 mmol) in MeOH (10 ml) at 0° C. The reaction mixture was stirred at 0° C. for 30 min, stirred at rt for 1 hr, then quenched by the dropwise addition of H2O (1.0 ml). The resulting mixture was concentrated in vacuo to remove the methanol, and the remaining aqueous layer was extracted with CHCl3 (4×10 ml). The combined extracts were dried over MgSO4 and concentrated in vacuo to give 0.138 g (99% yield) of colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06608203B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-74bfd9601ac04e8c89d128cfd1fcc695 |
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| Source note | uspto-grants-2003_08 |
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