HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375205Generated: October 31, 2026
Trifluoroacetic acid → HCID 131726212, compound
https://huagongshe.com/reaction/1375205
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 2-(2-{[(Tert-butoxy)carbonyl]amino}acetamido)acetic acid | HCID 333466 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131726212 | HCID 131726212 | — |
Reaction Steps
A 100 mL media bottle equipped with a septum cap and stir bar was charged with of t-BOC-GlyGly-Ama-diEt (5.12 g, 13.14 mmol) and CH2Cl2(15 mL). With vigorous stirring, TFA (25 mL in 25 mL CH2Cl2) was added dropwise. After 1 hour the reaction was complete, the TFA was removed in vacuo and the trifluoroacetate salt precipitated with Et2O. The TFA-GlyGly-Ama-diEt salt was collected by filteration, washed with Et2O and recrystallized from absolute EtOH:ether (7:3 v/v). The white crystals were dried in vacuo to give 5.21 g of product: 1H NMR (DMSO-d6) δ 8.96 (br d, 1, —NHCH—), 8.63 (br t, 1, —NHCH2—), 8.02 (v br s, 3, NH3CH2), 5.09 (d, 1, CH(CO2Et), 4.12−4.24 (m, 4, OCH2CH3), 3.94 (br d, 2, —NHCH2—), 3.59 (br s, 2, —NHCH2—), 1.21 (t, 6, OCH2CH3). 13C NMR (CDCl3) δ 168.8, 166.4, 158.3, 158.0, 119.3, 115.4, 61.9, 56.3, 41.5, 13.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07166733B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-1bc5135485cd4e0f820e5af531ee6094 |
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| Source note | uspto-grants-2007_01 |
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