HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397045Generated: October 29, 2026
Sodium borohydride → HCID 18172397, compound
https://huagongshe.com/reaction/397045
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 18172454 | HCID 18172454 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 18172397 | HCID 18172397 | 93.5% |
Reaction Steps
Sodium borohydride (0.512 g, 13.5 mmol) was added in small portions to a solution of 1-cyclohexyl-6-methoxy-3,4-dihydroisoquinoline (0.822 g, 3.38 mmol) in MeOH (40 ml) at 0° C. The reaction mixture was stirred at 0° C. for 30 min, warmed to rt and stirred at rt for 15 hr, then quenched by the dropwise addition of H2O (5.0 ml). The resulting mixture was concentrated in vacuo to remove the MeOH and the remaining aqueous solution was extracted with CHCl3 (4×10 ml). The combined extracts were dried over MgSO4 and concentrated in vacuo to give 0.775 g (93% yield) of yellow 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-acb3efe5a6e94145ab4eb842b83928a6 |
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| Source note | uspto-grants-2003_08 |
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