HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927698Generated: October 31, 2026
Hydrochloric Acid → 5-[(N-Methyl-N-butylamino)carbonyl]-2,4-bisbenzyloxybenzoic acid
https://huagongshe.com/reaction/1927698
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Methyl 5-[(N-methyl-N-butylamino)carbonyl]-2,4-bisbenzyloxybenzoate | HCID 59614016 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-[(N-Methyl-N-butylamino)carbonyl]-2,4-bisbenzyloxybenzoic acid | HCID 59614060 | — |
Reaction Steps
59 g (127.8 mmol) of methyl 5-[(N-methyl-N-butylamino)carbonyl]-2,4-bisbenzyloxybenzoate are dissolved in 200 ml of THF and added to a solution of 100 g (4.2 mol) of lithium hydroxide in 300 ml of water and 150 ml of methanol. The mixture is stirred for 12 h at 22° C., diluted with 250 ml of diethyl ether and acidified using 1N hydrochloric acid. The organic phase is separated off and washed a further three times with 100 ml of N hydrochloric acid each time, dried over sodium sulfate and evaporated. The crude product obtained in this way (80 g) is crystallised from ethyl acetate: 33 g (57.7%) of 5-[(N-methyl-N-butylamino)carbonyl]-2,4-bisbenzyloxybenzoic acid (white crystals); MW 447.5;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08183279B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-088ff8a45a754a84b2c0a5db81885cac |
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| Source note | uspto-grants-2012_05 |
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