HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671622Generated: October 31, 2026
4-Chlorobenzaldehyde → HCID 25209039, compound
https://huagongshe.com/reaction/1671622
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chlorobenzaldehyde | HCID 7726 | — |
| Reactant | L-Alaninol | HCID 80307 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 25209039 | HCID 25209039 | — |
Reaction Steps
4-Chloro-benzaldehyde (1.4 g, 0.01 mol) was dissolved in dry ethanol (30 mL) and (S)-(+)-2-amino-1-propanol (0.75 g, 0.01 mol) was added. The reaction mixture was stirred overnight at 60° C. The ethanol was evaporated under reduced pressure to give a colorless oil. The oil was then dissolved in dry methanol (30 mL) and cooled in ice. NaBH4 (0.57 g, 0.015 mol) was added slowly in portions, and the resulting solution was left overnight at room temperature. The solvent was evaporated in vacuo, and the residue was dissolved in water, and extracted with CH2Cl2 (3×20 mL). The organic layers were combined and dried with Na2SO4, filtered and evaporated in vacuo to give colorless oily residue, which was purified by column chromatography (silica gel, CH2Cl2:MeOH, 9:1) to afford colorless oil (III-1, 1.85 g, 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07994326B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-505e3e3f79ef4bfd85733365d59bdbef |
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| Source note | uspto-grants-2011_08 |
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