Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734227Generated: October 25, 2026

Tert-Butyl hypochlorite → Phenylmethyl 2-({[(1,1-dimethylethyl)oxy]carbonyl}amino)-3-hydroxy-8-azaspiro[4.5]decane-8-carboxylate

https://huagongshe.com/reaction/734227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-Butyl hypochloriteHCID 521297—
ReactantBoc-carbamateHCID 57418545—
ReactantPhenylmethyl 8-azaspiro[4.5]dec-2-ene-8-carboxylateHCID 69055893—
Solvent1-PropanolHCID 1031—
SolventSodium HydroxideHCID 14798—
ProductPhenylmethyl 2-({[(1,1-dimethylethyl)oxy]carbonyl}amino)-3-hydroxy-8-azaspiro[4.5]decane-8-carboxylateHCID 69054060103.6%

Reaction Steps

To a solution of Boc-carbamate (2.68 g, 22.9 mmol) in nPrOH (70 mL) at 25° C. was added an NaOH solution (32 mL, prepared from 900 mg of NaOH in 37 mL H2O) followed by tBuOCl (2.58 mL, 22.51 mmol). After 15 min, phenylmethyl 8-azaspiro[4.5]dec-2-ene-8-carboxylate (2 g, 7.4 mmol) in nPrOH (3 mL) was added followed by K2OsO2(OH)2 (109 mg, 0.295 mmol) dissolved in the remaining NaOH solution prepared above (5 mL). After 1 h, the solution was extracted with EtOAc, concentrated and purified via column chromatography (1-7% MeOH in DCM (1% NH4OH)) yielding the title compound (˜3.1 g, contaminated with residual Boc-carbamate) as a white solid: LCMS (ES) m/e 405 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592334B2
Source datasetuspto-grants-2009_09
ORD IDord-0f54e5cbb9a04e4f8dfa56cef40c880e
Source noteuspto-grants-2009_09