HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855190Generated: October 29, 2026
4-tert-Butylbenzaldehyde → HCID 68696866, compound
https://huagongshe.com/reaction/855190
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-tert-Butylbenzaldehyde | HCID 70324 | — |
| Reactant | 2-(2-Chlorophenyl)ethylamine | HCID 83117 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68696866 | HCID 68696866 | 97% |
Reaction Steps
0.38 ml of 4-tert-butylbenzaldehyde (2.25 mmol) and 0.215 ml 2-(2-chloro-phenyl)-ethylamine (1.5 mmol) were dissolved in 4.5 ml methanol at rt, and after stirring for 30 min at rt, were refluxed for 2.5 h. After cooling down to rt, 85 mg (2.25 mmol) sodium borohydride were added and after stirring for 5 min at rt, the reaction mixture was then refluxed for 3 h. After cooling down to rt, the reaction mixture was treated with 4 drops 1 N HCl and concentrated in vacuo. The residue was diluted with water/EtOAc. After separation of the organic phase, the aqueous phase was extracted with EtOAc and the combined organic phases were washed with brine, dried with magnesium sulfate, filtered off and concentrated in vacuo. The residue was purified by column chromatography (40 g silica gel; EtOAc/heptane 1:2) to give 465 mg light yellow oil (97%). MS (ISP) 302.3 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07259183B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-785b7d9f1abc42beb5c1cf4b93b46207 |
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| Source note | uspto-grants-2007_08 |
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