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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624302Generated: November 1, 2026

Chloroiodomethane → HCID 69156419, compound

https://huagongshe.com/reaction/1624302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroiodomethaneHCID 11644—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 11218203HCID 11218203—
ReactantHCID 178418750HCID 178418750—
SolventDichloromethaneHCID 6344—
ProductHCID 69156419HCID 6915641997.2%

Reaction Steps

To a cold (0° C.), stirred solution of diethyl zinc (1.0 M in hexanes, 4.0 mL, 4.0 mmol) in CH2Cl2 (8 mL) was added neat ClCH2I (0.58 mL, 7.96 mmol) drop wise by syringe. After 1 hour, a solution of 4-(tert-butyldimethylsilyloxy)-2-methylene-butan-1-ol (0.395 g, 1.83 mmol) in CH2Cl2 (4 mL) was added by cannula. After 30 minutes, the reaction mixture was treated with saturated aqueous NH4Cl (10 mL), diluted with CH2Cl2 (12 mL), and warmed to room temperature. The phases were separated and the aqueous phase was extracted with CH2Cl2 (3×10 mL). The combined organic extracts were dried (Na2SO4) and concentrated. The crude material was purified by column chromatography on silica gel (9:1 hexanes-ethyl acetate) and provided 0.41 g (97%) of {1-[2-(tert-butyldimethylsilyloxy)-ethyl]-cyclopropyl}-methanol as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778967B2
Source datasetuspto-grants-2014_07
ORD IDord-b357184b70bc4837856eb44b9ca161a9
Source noteuspto-grants-2014_07