HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482843Generated: October 30, 2026
Hydrochloric Acid → HCID 86736761, compound
https://huagongshe.com/reaction/482843
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 86736762 | HCID 86736762 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86736761 | HCID 86736761 | 74.7% |
Reaction Steps
2-[3-{4-(3-tert-butoxycarbonylamino-3-methoxycarbonylpropoxy)phenylglyoxyloylamino}-2-oxo-1-azetidinyl]-2-(2-thienyl)acetic acid (0.480 g.) was dissolved in methanol (3 ml.), and to the solution, there was added 1 N aqueous sodium hydroxide (2 ml.) under ice-cooling. The mixture was stirred at the same temperature for 7 hours while adjusting to pH 9.0 to 9.5 with 1 N aqueous sodium hydroxide. After the reaction, the reaction mixture was adjusted to pH 7.0 with dilute hydrochloric acid and evaporated to dryness under reduced pressure on a water bath. The resultant residue was dissolved in a small amount of water, and the aqueous solution was adjusted to pH 5.5 with dilute hydrochloric acid and then washed with ethyl acetate. The aqueous solution was adjusted to pH 4.0 to 4.5 with dilute hydrochloric acid and then extracted with ethyl acetate. This extract was evaporated to dryness under reduced pressure to give 2-[3-{4-(3-tert-butoxycarbonylamino-3-carboxypropoxy)phenylglyoxyloylamino}-2-oxo- 1-azetidinyl]-2-(2-thienyl)acetic acid (0.350 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04576753 |
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| Source dataset | uspto-grants-1986_03 |
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| ORD ID | ord-25d90799ec6a48f3b86c6ed68c06f24f |
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| Source note | uspto-grants-1986_03 |
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