HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182092Generated: October 25, 2026
Imidazole → Benzyl (S)-3-(Boc-amino)-4-iodobutanoate
https://huagongshe.com/reaction/1182092
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Phenylmethyl (3S)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxybutanoate | HCID 10040985 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl (S)-3-(Boc-amino)-4-iodobutanoate | HCID 11258642 | — |
Reaction Steps
A suspension of polymer bound triphenyl phosphine (18.25 g, 54.76 mmol) in DCM (100 ml) is treated with iodine (12.2 g, 48.1 mmol) and the reaction mixture stirred at ambient temperature for 15 minutes. Imidazole (3.72 g, 54.7 mmol) is added and the reaction mixture stirred for a further 15 minutes. A solution of (S)-3-tert-butoxycarbonylamino-4-hydroxy-butyric acid benzyl ester (6.76 g, 21.9 mmol) in DCM (100 ml) is added. The suspension is stirred at reflux for 1.5 hours, then filtered through Celite™ filter material, washing through with DCM. The combined organic phase is washed with an aqueous solution of 10% sodium thiosulphate, water and brine, then dried over magnesium sulphate and evaporated. The crude product is chromatographed over flash silica using 8% ethylacetate in iso-hexane as eluent to afford (S)-3-tert-butoxycarbonylamino-4-iodo-butyric acid benzyl ester. [M-BOC] 320.12
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07288537B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-03e7a4abcdd845eca11b0eb3e0bc38af |
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| Source note | uspto-grants-2007_10 |
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