HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620302Generated: October 29, 2026
Hydrochloric Acid → HCID 19818635, compound
https://huagongshe.com/reaction/620302
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 19818646 | HCID 19818646 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 19818635 | HCID 19818635 | — |
Reaction Steps
18 ml of N sodium hydroxide solution are added to a solution of 7.95 g of methyl N-{{4-{3-[4-acetyl-3-hydroxy-2-(3,3,3-trifluoropropyl)-phenoxy]-propoxy]-3-methoxy-phenyl}}-oxamate in 100 ml of methanol and the mixture is refluxed for 1 hours. The hot solution is then poured into 200 ml of 0.1N hydrochloric acid. The product which has precipitated out is filterred off, washed with water and dried over phosphorus pentoxide in a drying cabinet. The N-{{4-{3-[4-acetyl-3-hydroxy-2-(3,3,3-trifluoropropyl)-phenoxy]-propoxy}-3-methoxy-phenyl}}-oxamic acid thus obtained is dissolved hot again in 100 ml of methanol, and one equivalent of triethanolamine in 10 ml of methanol is added. After addition of 400 ml of ether, crystallisation starts. The treithanolammonium salt of N-{{4-{3-[4-acetyl-3-hydroxy-2-(3,3,3-trifluoropropyl)-phenoxy]-propoxy}-3-methoxy-phenyl}}-oxamic acid is thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04820726 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-216fc180fb2940a7bb3556110df1f559 |
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| Source note | uspto-grants-1989_04 |
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