HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106300Generated: October 30, 2026
Trifluoroacetic acid → HCID 131712661, compound
https://huagongshe.com/reaction/1106300
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 3a,4,7,7a-Tetrahydro-2-hydroxy-4,7-methano-1H-isoindole-1,3(2H)-dione | HCID 89529 | — |
| Reactant | Boc-Met(O)-Oh | HCID 7408090 | — |
| Reactant | HCID 131711783 | HCID 131711783 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131712661 | HCID 131712661 | — |
Reaction Steps
To 50.0 g of Boc-Asn-Thr-OBzl is added 170 ml of TFA and the mixture is shaken at room temperature for 30 minutes. The solution is concentrated and treated with 500 ml of diethyl ether. The resultant powder is collected by filtration and dried. It is dissolved in 400 ml of THF, and under ice-cooling 20 ml of TEA is added. To this solution is added Boc-Met(O)-ONB (prepared by dissolving 31.3 g of Boc-Met(O).OH and 23.3 g of HONB in 200 ml of THF, adding 26.8 g of DCC under ice-cooling and stirring the mixture for 4 hours). The mixture is stirred for 15 hours, after which time the solvent is distilled off under reduced pressure. To the residue are added ethyl acetate (200 ml) and ether (200 ml), and the resultant powders are collected by filtration and reprecipitated from acetonitrile. Yield 48.5 g (72.0%), m.p. 145°-147° C., [α]D23 -6.5° (c=1.1, DMF), Rf1 =0.19.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04312943 |
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| Source dataset | uspto-grants-1982_01 |
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| ORD ID | ord-0c03792db83547caa4a55fd3570e1609 |
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| Source note | uspto-grants-1982_01 |
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