HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845485Generated: October 30, 2026
Hydrochloric Acid → HCID 53987327, compound
https://huagongshe.com/reaction/845485
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 4-(4-Methoxyphenyl)butyric acid | HCID 78280 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 53987327 | HCID 53987327 | — |
Reaction Steps
To a solution of lithium diisopropylamide (prepared from diisopropylamine (16.16 g, 0.16 mol and n-butyl lithium (1.6M in hexane, 100 ml, 0.016 mol) in THF (50 ml) at -78° C., was added a solution of 4-(4-methoxyphenyl)butanoic acid (13.80 g, 0.07 mol) in THF (100 ml) over 20 min. The solution was warmed to -20° C. and stirred for 2.5 h. Formaldehyde gas generated by warming paraformaldehyde (10 g) was then passed into the reaction mixture in a stream of nitrogen. After stirring for a further 2 h. at -20° C., hydrochloric acid (2N, 500 ml) was added and the reaction mixture was diluted with ethyl acetate (800 ml). After washing with water, the organic phase was extracted with sodium hydroxide solution (0.5N, 3×200 ml). The combined aqueous extracts were acidified with hydrochloric acid and extracted with ethyl acetate (3×200 ml), the combined organic phase (MgSO4) was dried and solvent removed at reduced pressure to give the product as a colourless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04758573 |
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| Source dataset | uspto-grants-1988_07 |
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| ORD ID | ord-097f31c8678f4f648275c447cc73f2e8 |
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| Source note | uspto-grants-1988_07 |
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