HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182122Generated: October 26, 2026
Imidazole → ((s)-3-Iodo-1-methoxymethyl-propyl)-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/1182122
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | tert-Butyl (S)-(4-hydroxy-1-methoxybutan-2-yl)carbamate | HCID 53259998 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ((s)-3-Iodo-1-methoxymethyl-propyl)-carbamic acid tert-butyl ester | HCID 86600851 | — |
Reaction Steps
A suspension of polystyrene resin-bound triphenylphosphine (18.645 g, 3 mmol/g) in dry dichloromethane (250 ml) is treated with iodine (12.5 g, 49.22 mmol) and stirred for 15 minutes under argon. Imidazole (3.87 g, 55.94 mmol) is added and the reaction mixture stirred at room temperature for a further 15 minutes. The reaction mixture is then treated with a solution of ((S)-3-Hydroxy-1-methoxymethyl-propyl)-carbamic acid tert-butyl ester (4.9 g, 22.37 mmol) in dichloromethane (30 ml), and refluxed for 1.5 hours under argon. The resin is removed by filtration through a celite pad, washing with dichloromethane. The filtrate is washed with 5% aqueous sodium thiosulphate solution and water, dried over MgSO4 and evaporated to afford ((S)-3-Iodo-1-methoxymethyl-propyl)-carbamic acid tert-butyl ester as a crude oil. [M-BOC] 230.06.
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-75e5c7ae8e85446c9f4e6571ebc35a00 |
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| Source note | uspto-grants-2007_10 |
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