HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880492Generated: October 27, 2026
Sodium borohydride → Methyl N-{(4-bromophenyl)[4-(methylsulfonyl)phenyl]methyl}-L-leucinate
https://huagongshe.com/reaction/1880492
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (4-Bromophenyl)(4-(methylsulfonyl)phenyl)methanone | HCID 21262853 | — |
| Reactant | methyl N-{(4-bromophenyl)[4-(methylsulfonyl)phenyl]methylene}leucinate | HCID 86590539 | — |
| Solvent | Acetic acid methanol | HCID 10129899 | — |
| Product | Methyl N-{(4-bromophenyl)[4-(methylsulfonyl)phenyl]methyl}-L-leucinate | HCID 67298353 | — |
Reaction Steps
To a solution of a 1:1 mixture of methyl N-{(4-bromophenyl)[4-(methylsulfonyl)phenyl]methylene}leucinate and (4-bromophenyl)[4-(methylsulfonyl)phenyl]methanone from step 1 (185 mg, ˜0.2 mmol) in acetic acid/methanol (1:3, 4 mL) was added sodium borohydride (˜400 mg) by portions every 30 min over 2 days (addition was stopped during the night) using a solid addition funnel. The reaction mixture was partitioned between EtOAc and water, the organic layer was dried over Na2SO4 and concentrated. The resulting mixture was purified by chromatography using EtOAc and hexane as eluant. Methyl N-{(4-bromophenyl)[4-(methylsulfonyl)phenyl]methyl}-L-leucinate was obtained as a colorless gum and (4-bromophenyl){4-(methylsulfonyl)phenyl}methanol was obtained as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318748B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-2d5ef937894a4dfe9838b58486594457 |
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| Source note | uspto-grants-2012_11 |
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