HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292342Generated: November 2, 2026
Trifluoroacetic acid → HCID 178460210, compound
https://huagongshe.com/reaction/2292342
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | HCID 178460209 | HCID 178460209 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178460210 | HCID 178460210 | — |
Reaction Steps
To a suspension of 10.83 g (13.6 mmol) of the crude [[[[[(S)-3-[[(Z)-(2-amino-4-thiazolyl)[(2-carboxy-2-methylethoxy)imino]acetyl]amino]-2-oxo-1-azetidinyl]carbonyl]amino]sulfonyl]amino]-3,4-dihydroxybenzeneacetic acid, diphenylmethyl ester in 45 ml of dry dichloromethane at -10° C., a cold solution of 11 ml of anisole in 110 ml of trifluoroacetic acid was added. After being stirred at 0° C. for 10 minutes, the clear solution was evaporated in vacuo at 0°-5° C. and the residue was treated with dry ether. The solid was collected by suction, washed with dry ether, dried in vacuo to give 7.28 g of impure [[[[[(S)-3-[[(Z)-(2-amino-4-thiazolyl)[(2-carboxy-2-methylethoxy)imino]acetyl]amino]-2-oxo-1-azetidinyl]carbonyl]amino]sulfonyl]amino]-3,4-dihydroxybenzeneacetic acid, trifluoroacetate salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04801705 |
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| Source dataset | uspto-grants-1989_01 |
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| ORD ID | ord-bf767defe7964b1c8875609ddc0ee1c6 |
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| Source note | uspto-grants-1989_01 |
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