HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 931901Generated: October 30, 2026
Lithium borohydride → HCID 67999428, compound
https://huagongshe.com/reaction/931901
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | (S)-ethyl 2-((3R,5R,6S)-3-(2-tert-butoxy-2-oxoethyl)-5-(3-chlorophenyl)-6-(4-chlorophenyl)-2-oxopiperidin-1-yl)butanoate | HCID 86660716 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 67999428 | HCID 67999428 | — |
Reaction Steps
To a solution of (S)-ethyl 2-((3R,5R,6S)-3-(2-tert-butoxy-2-oxoethyl)-5-(3-chlorophenyl)-6-(4-chlorophenyl)-2-oxopiperidin-1-yl)butanoate (1.94 g, 3.54 mmol, Example 21, Step A) in Et2O (35.4 mL) was added 90% lithium borohydride (0.154 g, 7.07 mmol) at 0° C. After being stirred at 0° C. for 30 min, the reaction was quenched (ice cold 10% citric acid), extracted (2×EtOAc) and washed (sat. aq. NaCl solution). The combined organic layers were washed with sat. NaCl solution, dried over Na2SO4, filtered and the filtrate was concentrated under reduced pressure. Purification by chromatography on silica gel (50% to 100% EtOAc/Hexanes, gradient elution) provided the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09296736B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-9ef676b7efed425c9debacb92be5231b |
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| Source note | uspto-grants-2016_03 |
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