HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096169Generated: October 27, 2026
Chloroiodomethane → (4S)-6-Azaspiro[2.5]octan-4-ol hydrochloride
https://huagongshe.com/reaction/1096169
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroiodomethane | HCID 11644 | — |
| Reactant | tert-Butyl 3-hydroxy-4-methylidenepiperidine-1-carboxylate | HCID 10584700 | — |
| Reactant | HCID 178418750 | HCID 178418750 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | (4S)-6-Azaspiro[2.5]octan-4-ol hydrochloride | HCID 44541812 | 36,664.699% |
Reaction Steps
To a solution of diethylzinc (1.1 M solution in toluene, 37.5 ml, 0.04 mmol) in DCE (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 DCE (10 ml) was added, after which time the reaction was stirred for 0.5 h at 0° C. and then allowed to reach RT, stirring for a further 1 h. The reaction was then quenched by addition of sat. aq. ammonium chloride solution, separated, and the organic dried (Na2SO4) and concentrated. Purification by flash column chromatography (EtOAc/heptane 2:8→1:1) afforded the title product (2.4 g, 54%) as a crystalline solid. MS: 228.2 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08138175B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-a0526033810b456a9d18ec2fcec36d06 |
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| Source note | uspto-grants-2012_03 |
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