HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253989Generated: November 1, 2026
Trifluoroacetic acid → HCID 59997296, compound
https://huagongshe.com/reaction/1253989
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 59997228 | HCID 59997228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59997296 | HCID 59997296 | 99.2% |
Reaction Steps
To an ice cold solution of tert-Butyl (1S,2R)-3-[(1,3-benzodioxol-5-ylsulfonyl) (1-ethylpropoxy)amino]-1-[4-(benzyloxy)benzyl]-2-hydroxypropylcarbamate (1.5 g, 2.3 mmol) in dichloromethane (15 mL) was added trifluoroacetic acid (10 mL). After stirring at 5° C. for 3 h, the reaction was concentrated in vacuo, taken up in ethyl acetate (80 mL), washed with saturated sodium bicarbonate (2×50 ml), dried (magnesium sulfate) and concentrated in vacuo to afford the title compound (1.27 g, quant.) as an off-white foam. 1H NMR (DMSO-d6): δ 0.77 (6H, dt), 1.07-1.72 (4H, m), 1.82 (2H, br), 2.28 (1H, t), 2.58-3.05 (4H, m), 3.43-3.53 (1H, m), 3.95-4.03 (1H, m), 4.86 (1H, br s), 5.01 (2H, s), 6.16 (2H, s), 6.86 (2H, d), 7.03 (2H, d), 7.12-7.40 (8H, m);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08455497B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-354f0515412d4fb681811c57e55dff92 |
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| Source note | uspto-grants-2013_06 |
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