HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398003Generated: October 29, 2026
Sodium borohydride → HCID 11080708, compound
https://huagongshe.com/reaction/398003
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 23001298 | HCID 23001298 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11080708 | HCID 11080708 | — |
Reaction Steps
The product from Example 1, Step A (8.87 g, 20.2 mmol) was dissolved in methanol (50 mL) and methylene chloride (20 mL). Sodium borohydride (764 mg, 20.2 mmol) was added in portions at 0° C., and the solution was stirred for 2 hours. The reaction was quenched by the addition of saturated aqueous ammonium chloride until hydrogen evolution ceased. The resulting suspension was concentrated in vacuo and then partitioned between methylene chloride (50 mL) and saturated aqueous sodium bicarbonate (50 mL). The layers were separated and the aqueous layer was extracted with methylene chloride (3×100 mL). The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo to provide the title product as a yellow oil which was sufficiently pure for use in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06610722B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-d025209c2ceb469c87a959de64c4e453 |
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| Source note | uspto-grants-2003_08 |
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