HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591315Generated: November 1, 2026
Water → (2S)-2-tert.-Butoxycarbonylamino-5-{2-[4-(2-fluoro-ethoxy)-phenyl]-ethyl}-hexanedioic acid di-tert.-butyl ester
https://huagongshe.com/reaction/591315
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethane, 1-fluoro-2-iodo- | HCID 69804 | — |
| Reactant | Di-tert-butyl (2S)-2-[(tert-butoxycarbonyl)amino]-5-[2-(4-hydroxyphenyl)ethyl]hexanedioate | HCID 70977973 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (2S)-2-tert.-Butoxycarbonylamino-5-{2-[4-(2-fluoro-ethoxy)-phenyl]-ethyl}-hexanedioic acid di-tert.-butyl ester | HCID 89156295 | 60.2% |
Reaction Steps
53 mg (0.30 mmol) 1-Fluoro-2-iodoethane were dissolved in 5 ml dimethylformamide 98 mg (0.71 mmol) potassium carbonate and 100 mg (0.20 mmol) (2S,5RS)-2-tert.-Butoxycarbonylamino-5-[2-(4-hydroxy-phenyl)-ethyl]-hexanedioic acid di-tert.-butyl ester added. The mixture was stirred at room temperature over night. For workup, water and ethyl acetate were added, the phases separated and the water extracted with ethyl acetate twice. Combined organic phases were dried (Na2SO4), filtered and evaporated. The raw product was absorbed on Isolute and chromatographed on a Biotage Isolera system (SNAP NH 110 g, A=n-hexane, B=ethyl acetate, A 2 CV, A to 47% B in 9.4 CV, 5 CV 50% B, 50 mL/min, Fr. a 22 mL). Fractions 29 to 32 were collected to give 65 mg (59%) of (2S,5RS)-2-tert.-Butoxycarbonylamino-5-{2-[4-(2-fluoro-ethoxy)-phenyl]-ethyl}-hexanedioic acid di-tert.-butyl ester as clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238631B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-83526803008c4e6a90721946b4dcf299 |
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| Source note | uspto-grants-2016_01 |
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