HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165271Generated: October 30, 2026
Trifluoroacetic acid → HCID 131716454, compound
https://huagongshe.com/reaction/2165271
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | HCID 86744080 | HCID 86744080 | — |
| Product | HCID 131716454 | HCID 131716454 | — |
Reaction Steps
(3S-trans)-[[3-[(t-Butyloxycarbonyl)amino]-4-methyl-2-oxo-1-azetidinyl]oxy]acetic acid. diphenylmethyl ester (4.4 g1 10.0 mmol) was dissolved in a solution of 33 ml of trifluoroacetic acid and anisole (3.3 ml; 30.0 mmol) at -10° C. The mixture was evaporated in vacuo 10 minutes later and the residue was stirred with ether, filtered off and dried over P2O5 to give colorless crystals of (3S)-[[3-amino-4-methyl-2-oxo-1-azetidinyl]oxy]acetic acid, trifluoroacetate salt (yield 2.87 g). The salt (2.87 g; 10.0 mmol) was suspended in dry acetonitrile. MSTFA (5.57 ml; 30.0 mmol) was added and stirring was continued for 30 minutes. After evaporating in vacuo the residue was dissolved in dry tetrahydrofuran and then added to a mixture of the [[[(4-methoxyphenyl)methoxy]-carbonyl]amino]benzeneacetic acid 1-hydroxybenzotriazole ester (4. g, 10.0 mmol) in 25 ml of dry tetrahydrofuran at 0° C., stirred overnight at room temperature and evaporated in vacuo. After adding ether the crude silylated product was decomposed with 1 ml methanol. After removing the solvents in vacuo the residue was stirred with ether/petroleum ether to give colorless crystals of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04939253 |
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| Source dataset | uspto-grants-1990_07 |
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| ORD ID | ord-97d3dfaaadbb4398918d50ab91c8cfec |
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| Source note | uspto-grants-1990_07 |
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