HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489044Generated: October 30, 2026
Chloroiodomethane → HCID 23387569, compound
https://huagongshe.com/reaction/489044
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroiodomethane | HCID 11644 | — |
| Reactant | Tetrabutylammonium Hydroxide | HCID 2723671 | — |
| Reactant | HCID 23405699 | HCID 23405699 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 23387569 | HCID 23387569 | — |
Reaction Steps
To a solution of 4-(N-benzyloxycarbonyl-L-valyloxy)cyclohexanoic acid (6.6 g, 20 mmole) in 1,4-dioxane (70 ml) was added a 40% solution of tetrabutylammonium hydroxide (11.34 g, 17.5 mmole) and the mixture was stirred 2 hours at room temperature. The mixture was evaporated under reduced pressure and co-evaporated two times with 1,4-dioxane and two times with toluene. The dried product was dissolved in 60 ml dichloromethane and iodochloromethane (30.9 g, 175 mmole) was added. The solution was stirred for two days at room temperature and evaporated under reduced pressure. About 100 ml ethyl actate was added and the organic phase washed twice with water, dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with toluene/acetone. Yield: 4.1 g=55%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06974802B2 |
|---|
| Source dataset | uspto-grants-2005_12 |
|---|
| ORD ID | ord-682526d6a61f452eab1c5a30108522c8 |
|---|
| Source note | uspto-grants-2005_12 |
|---|