HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610739Generated: October 29, 2026
Sodium borohydride → HCID 86593309, compound
https://huagongshe.com/reaction/1610739
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 22262346 | HCID 22262346 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 86593309 | HCID 86593309 | 81% |
Reaction Steps
To a suspension (60 ml) of zinc chloride (4.75 g, 34.8 mmol) in ether was added sodium borohydride (2.64 g, 69.6 mmol) at room temperature, and the mixture was stirred as it was for 2 hrs. Insoluble material was filtered off. To the filtrate was added a solution of ethyl 2-[3-(neopentyloxy)benzyl]-3-(3-chlorophenyl)-3-oxopropionate (2.64 g, 69.6 mmol) in ether (40 ml), and the mixture was stirred at room temperature for 1 hr. The reaction was quenched with 1N hydrochloric acid. The mixture was diluted with ethyl acetate, washed with water and saturated brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=8:1, 3:1) to give ethyl (2RS,3RS)-2-[3-(neopentyloxy)benzyl]-3-(3-chlorophenyl)-3-hydroxypropionate (5.82 g, 81%) as a colorless transparent oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06982348B2 |
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| Source dataset | uspto-grants-2006_01 |
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| ORD ID | ord-83048803da944ded947a930831609db2 |
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| Source note | uspto-grants-2006_01 |
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