HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591256Generated: October 30, 2026
Potassium Carbonate → Di-tert-butyl (4S)-N-(tert-butoxycarbonyl)-4-[4-(3-fluoropropoxy)benzyl]-L-glutamate
https://huagongshe.com/reaction/591256
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Iodo-3-fluoropropane | HCID 12899128 | — |
| Reactant | di-tert-butyl (4S)-N-(tert-butoxycarbonyl)-4-(4-hydroxybenzyl)-L-glutamate | HCID 70957078 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Di-tert-butyl (4S)-N-(tert-butoxycarbonyl)-4-[4-(3-fluoropropoxy)benzyl]-L-glutamate | HCID 70674426 | — |
Reaction Steps
To 93 mg (0.20 mmol) of di-tert-butyl (4S)—N-(tert-butoxycarbonyl)-4-(4-hydroxybenzyl)-L-glutamate (Example 1b) in 9 mL N,N-dimethylformamide were added 60.7 mg (0.44 mmol) of powdered potassium carbonate and 45 mg (0.24 mmol) of 1-iodo-3-fluoropropane (ABCR GmbH, Germany) and the resulting suspension was stirred for 5 h at 60° C. and overnight at room temperature. The reaction mixture was than filtered, the solvent evaporated and the residue was taken up in ethyl acetate and water. The organic phase was separated off, washed with water until neutral, dried over sodium sulfate and filtered, and the filtrate was concentrated in vacuo. The crude product obtained in this manner was chromatographed on silica gel using a dichloromethane/methanol gradient, and the appropriate fractions were combined and concentrated.
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-82c6a512333d4a8daa38c41fb2626900 |
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| Source note | uspto-grants-2016_01 |
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