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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559329Generated: October 26, 2026

Chloroiodomethane → (4S)-6-Azaspiro[2.5]octan-4-ol hydrochloride

https://huagongshe.com/reaction/559329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroiodomethaneHCID 11644—
Reactanttert-Butyl 3-hydroxy-4-methylidenepiperidine-1-carboxylateHCID 10584700—
ReactantHCID 178418750HCID 178418750—
Solvent1,2-DichloroethaneHCID 11—
Product(4S)-6-Azaspiro[2.5]octan-4-ol hydrochlorideHCID 4454181236,664.699%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of diethylzinc (1.1 M solution in toluene, 37.5 ml, 0.04 mmol) in 1,2-dichloroethane (80 ml) at 0° C. was added chloroiodomethane (5.99 ml, 0.08 mmol) under Ar. This mixture was stirred for 15 minutes before a solution of 3-hydroxy-4-methylene-piperidine-1-carboxylic acid tert-butyl ester (J. Org. Chem. 2001, 66, 2487) (4.19 g, 19.6 mmol) in 1,2-dichloroethane (10 ml) was added, after which time the reaction was stirred for 0.5 h at 0° C. and then allowed to reach room temperature, stirring for a further 1 h. The reaction was then quenched by addition of saturated aq. ammonium chloride solution, separated, and the organic dried (Na2SO4) and concentrated. Purification by flash column chromatography (ethyl acetate/heptane 2:8-1:1) afforded the title product (2.4 g, 54%) as a crystalline solid MS: 228.2 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063042B2
Source datasetuspto-grants-2011_11
ORD IDord-2e7967a7a7c94bc5bac14bfffe51af8e
Source noteuspto-grants-2011_11