HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41663Generated: October 27, 2026
Sodium borohydride → [2-(4-Chlorophenyl)selenazol-5-yl]methanol
https://huagongshe.com/reaction/41663
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-(4-Chlorophenyl)selenazole-5-carbaldehyde | HCID 59562494 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | [2-(4-Chlorophenyl)selenazol-5-yl]methanol | HCID 59562443 | 97.1% |
Reaction Steps
To a suspension of 2-(4-chlorophenyl)selenazole-5-carbaldehyde (130 mg, 0.48 mmol) in methanol (5 ml) is added sodium borohydride (19 mg, 0.5 mmol) at 0° C. The reaction mixture is stirred at 0° C. for 0.5 hour. The reaction mixture is quenched with saturated aqueous ammonium chloride solution (10 ml), and extracted with dichloromethane (3×25 ml). The combined organic extracts are dried over anhydrous magnesium sulfate, filtered and the filtrate is evaporated to dryness to give [2-(4-chlorophenyl)selenazol-5-yl]methanol (127 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08530667B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-def5a08699b64282b99ab251b2ce304c |
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| Source note | uspto-grants-2013_09 |
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