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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579490Generated: October 29, 2026

Carbonic acid, bis(1,1-dimethylethyl) ester → Ethyl-2-allyl-2-(tert-butoxycarbonylamino)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hexanoate

https://huagongshe.com/reaction/579490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbonic acid, bis(1,1-dimethylethyl) esterHCID 10219638—
ReactantEthyl 2-allyl-2-amino-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hexanoateHCID 66833537—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
ProductEthyl-2-allyl-2-(tert-butoxycarbonylamino)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hexanoateHCID 6683333082%

Reaction Steps

A solution of ethyl 2-allyl-2-amino-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hexanoate (0.0897 g, 0.276 mmol) in ethyl acetate (0.6 mL, 0.5 M) and saturated aqueous NaHCO3 (0.6 mL) was treated with di-tert-butyl carbonate (0.090 g, 0.414 mmol) and stirred at room temperature. After 16 h, the layers were separated and the aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with saturated aqueous NaCl, dried over MgSO4, filtered and concentrated. Purification by MPLC (0-20% ethyl acetate in heptane over 6 CV) gave ethyl 2-allyl-2-(tert-butoxycarbonylamino)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hexanoate as a colorless oil (0.096 g, 82%). Rf 0.53 (30% ethyl acetate in heptane); ESI-LCMS m/z calcd for C22H40BNO6: 425.3. found 426.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040703B2
Source datasetuspto-grants-2015_05
ORD IDord-961072422f444ef5832b100cd4a6bb81
Source noteuspto-grants-2015_05