HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325345Generated: October 30, 2026
Tert-Butylamine → 4-[3-(tert-Butylamino)-2-hydroxypropoxy]benzaldehyde
https://huagongshe.com/reaction/325345
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | HCID 2736334 | HCID 2736334 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 4-[3-(tert-Butylamino)-2-hydroxypropoxy]benzaldehyde | HCID 12521586 | — |
Reaction Steps
To 4-(2,3-epoxypropoxy)benzaldehyde (20 g.) is added tert. butylamine (50 ml.) and the resulting solution is refluxed 17 hours. The excess tert. butylamine is removed by heating at atmospheric pressure to yield a solid residue. To this residue is added 6 N hydrochloric acid (200 ml.) and the resulting mixture is heated 5 hours on a steam bath. The solution is cooled and concentrated to 100 ml. on a steam bath under reduced pressure (20 mm. Hg.). The concentrated solution is made basic to pH 10 with saturated aqueous sodium carbonate and extracted with chloroform. The chloroform extract is concentrated to a solid which after recrystallization from acetonitrile yields 18 g. of 4-(3-tert.butylamino-2-hydroxypropxy)benzaldehyde, m.p. 123°-125.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04440774 |
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| Source dataset | uspto-grants-1984_04 |
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| ORD ID | ord-d13b5ee46724466eb636c8122a68cb2a |
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| Source note | uspto-grants-1984_04 |
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