HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602008Generated: October 30, 2026
Trifluoroacetic acid → HCID 22326974, compound
https://huagongshe.com/reaction/1602008
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | (2E)-5-(tert-Butyloxycarbonylamino)-5-methylhex-2-enoic acid | HCID 10847814 | — |
| Reactant | HCID 86587341 | HCID 86587341 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22326974 | HCID 22326974 | 36.5% |
Reaction Steps
To a solution of (2E)-5-(tert-butyloxycarbonylamino)-5-methylhex-2-enoic acid (0.5 g, 2.1 mmol) in dichloromethane (5 ml) was added trifluoroacetic acid (5 ml) and stirred for 60 min and concentrated in vacuo. Then a 10% aqueous solution of sodium carbonate (30 ml) and dioxane (30 ml) were added followed by 9H-fluorenylmethyl-succinimidyl carbonate (0.67 g, 2.1 mmol) and stirred overnight. The mixture was washed with petrol ether (2×20 ml) and the aqueous layer was acidified with 4N sulphoric acid (pH~3) and extracted with ethyl acetate (3×50 ml). The combined organic layers were washed with 1N sulfuric acid, water (4×20 ml), brine (20 ml), dried (Magnesiumsulfate) and concentrated in vacuo. The obtained product was precipitated from dichloromethane/ether and filtered to give 280 mg of (2E)-5-(((9H-flouren-9-yl)methoxy)carbonylamino)-5-methyl-hex-2-enoic acid, which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05977178 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-629097c8c26a40d2b874849b94bdf420 |
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| Source note | uspto-grants-1999_11 |
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