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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536590Generated: October 26, 2026

Beta-Aminoisobutyric Acid → tert-butyl (6S)-6-formyl-5-azaspiro[2.4]heptane-5-carboxylate

https://huagongshe.com/reaction/536590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBeta-Aminoisobutyric AcidHCID 64956—
ReactantTempoHCID 2724126—
Reactant(S)-Tert-butyl 6-(hydroxymethyl)-5-azaspiro[2.4]heptane-5-carboxylateHCID 66848415—
SolventDichloromethaneHCID 6344—
Producttert-butyl (6S)-6-formyl-5-azaspiro[2.4]heptane-5-carboxylateHCID 71743236—

Reaction Steps

To (S)-tert-butyl 6-(hydroxymethyl)-5-azaspiro[2.4]heptane-5-carboxylate (Intermediate 59, 2.2 g, 9.7 mmol) dissolved in 10 ml of DCM, TEMPO (306 mg, 1.9 mmol) and BAIB (3.43 mg, 10.6 mmol) were added. After 2 hours at 25° C., the reaction is diluted with DCM (150 ml), washed with an aqueous solution of Na2S2O3 then with water, dried (Na2SO4) and evaporated to obtain a crude that was purified by silica gel chromatography (petroleum ether to petroleum ether/ethylacetate 95/5). (S)-tert-butyl 6-formyl-5-azaspiro[2.4]heptane-5-carboxylate was obtained as light yellow solid (1.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859608B2
Source datasetuspto-grants-2014_10
ORD IDord-b2ae26e6f70c4220905d296676c2dadc
Source noteuspto-grants-2014_10