HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489095Generated: October 29, 2026
Chloroiodomethane → HCID 23387571, compound
https://huagongshe.com/reaction/489095
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroiodomethane | HCID 11644 | — |
| Reactant | Tetrabutylammonium Hydroxide | HCID 2723671 | — |
| Reactant | HCID 23387556 | HCID 23387556 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 23387571 | HCID 23387571 | 64.5% |
Reaction Steps
To a solution of 5-(N-CBz-L-valyloxy)-4-stearoyloxy-2,2-dimethylvaleric acid (16.0 g, 24 mmol) in dioxane (500 mL), was added dropwise a 40% aqueous solution of tetrabutylammonium hydroxide (14.3 mL). After stirring for 5 min, the solution was evaporated to dryness through co-evaporation with dioxane and toluene. The residue was dissolved in dichloromethane (500 mL) and then chloroiodomethane (17.5 mL, 240 mmol) was added and the solution was stirred for 6 h at room temperature. The solution was concentrated under reduced pressure and the residue was shaken with hexane/ethyl acetate (1:1 v/v, 400 mL). The yellow crystalline solid was filtered off and the filtrate was washed with aqueous solution of sodium thiosulfate (0.1 M) and the filtered through anhydrous sodium sulfate and evaporated to dryness. The residue was column chromatographed (silica gel, 1% MeOH in CH2Cl2), to give 11.0 g of chloromethyl 5-(N-CBz-L-valyloxy)4-stearoyloxy-2,2-dimethylvalerate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06974802B2 |
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| Source dataset | uspto-grants-2005_12 |
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| ORD ID | ord-d049bf67cfde4842af89b91233100312 |
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| Source note | uspto-grants-2005_12 |
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