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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174634Generated: October 31, 2026

Diiodomethane → HCID 86730688, compound

https://huagongshe.com/reaction/2174634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiiodomethaneHCID 6346—
ReactantSodium SulfateHCID 24436—
ReactantHCID 86730689HCID 86730689—
ReactantHCID 178418750HCID 178418750—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
ProductHCID 86730688HCID 8673068897%

Reaction Steps

A solution of 1-[(9Z,12Z)-octadeca-9,12-dien-1-yloxy]-3-(octyloxy)propan-2-ol in DCM (166 ml) in a 1 L flask under nitrogen was cooled in an ice/IPA bath (−15° C.) and then 1 M diethylzinc in hexane (199 ml, 199 mmol) added, followed by diiodomethane (24.05 ml, 298 mmol). The mixture was allowed to stir in the cooling bath overnight to gradually come up to room temperature. Reaction was quenched by addition of excess saturated ammonium chloride. Washed reaction into 2 L separatory funnel with hexane and water and added excess hexane, shook vigorously. Discarded lower aqueous layer, dried organic layer with sodium sulfate and evaporated to 1-(octyloxy)-3-[(8-{2-[(2-pentylcyclopropyl)methyl]cyclopropyl}octyl)oxy]propan-2-ol (15.5 g, 32.2 mmol, 97% yield) as a yellow oil. Material was used with no further purification. MS (ESI): 481 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062021B2
Source datasetuspto-grants-2015_06
ORD IDord-624ee9b673e64ea2b45f295751f271fb
Source noteuspto-grants-2015_06