HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1055602Generated: November 4, 2026
Sodium borohydride → HCID 131736399, compound
https://huagongshe.com/reaction/1055602
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (2R,3S,4S,5R,6S)-3,4,5-tribenzyloxy-6-[3-[(4-benzyloxyphenyl)methyl]-4-chloro-phenyl]-2-(hydroxymethyl)-6-methoxy-tetrahydropyran-2-carbaldehyde | HCID 131736398 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 131736399 | HCID 131736399 | 100% |
Reaction Steps
To a solution of (2R,3S,4S,5R,6S)-3,4,5-tribenzyloxy-6-[3-[(4-benzyloxyphenyl)methyl]-4-chloro-phenyl]-2-(hydroxymethyl)-6-methoxy-tetrahydropyran-2-carbaldehyde 25j (1.04 g, 1.3 mmol) in methanol (20 mL) was added sodium borohydride (98 mg, 2.6 mmol) slowly at 0° C. The mixture was stirred at 0° C. for 5 min. The reaction mixture was quenched with saturated aqueous ammonium chloride (15 mL) and extracted with ethyl acetate (50 mL×2). The combined organic layers were washed with water (30 mL×2) and saturated aqueous sodium chloride (30 mL×2) in turn, dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated in vacuo to give the title compound 25k as yellow oil (1.04 g, 100%). This material was not further purified.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09394329B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-4996c387890f47bb8f151fd79192f18c |
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| Source note | uspto-grants-2016_07 |
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