HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482286Generated: October 30, 2026
Trifluoroacetic acid → HCID 89668343, compound
https://huagongshe.com/reaction/1482286
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Silane, tris(1-methylethyl)- | HCID 138754 | — |
| Reactant | HCID 89668723 | HCID 89668723 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 89668343 | HCID 89668343 | 100% |
Reaction Steps
A solution of 2-(tert-butoxy)-2-oxoethyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)(methyl)amino)acetate (Fmoc-MeGly-HOGly-OtBu) (Compound SP637) (2.30 g, 5.41 mmol) in methylene chloride (18 mL) was mixed with triisopropylsilane (2.78 mL, 13.5 mmol) and trifluoroacetic acid (5.41 mL, 70.3 mmol) with stirring at room temperature, and the reaction mixture was stirred at room temperature for 2 hours. The reaction solution was concentrated under reduced pressure, and the resulting residue was purified by reverse-phase silica gel column chromatography (0.1% aqueous formic acid solution/0.1% formic acid-acetonitrile solution) to afford 2-(2-((((9H-fluoren-9-yl)methoxy)carbonyl)(methyl)amino)acetoxy)acetic acid (Fmoc-MeGly-HOGly-OH) (Compound SP638) (2.00 g, 5.41 mmol, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409952B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-145f95263eea4b21bdfcd4ad6628c5e5 |
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| Source note | uspto-grants-2016_08 |
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