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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643406Generated: November 1, 2026

(S)-tert-butyl 5,6-di(nitrooxy)hexanoate → (S)-5,6-di(nitrooxy)hexanoic acid

https://huagongshe.com/reaction/1643406

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-tert-butyl 5,6-di(nitrooxy)hexanoateHCID 59509520—
SolventDichloromethaneHCID 6344—
Product(S)-5,6-di(nitrooxy)hexanoic acidHCID 29923588—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (S)-tert-butyl 5,6-di(nitrooxy)hexanoate (12.41 g, 42.155 mmol) in DCM (47 mL) cooled to 0° C. under N2, boron trifluoride diethyl ether complex (5.82 mL, 46.37 mmol) was added. The reaction mixture was stirred at 0° C. for 10 minutes and at rt for 3 hrs. The solution was washed with brine, the organic layer was separated, dried over sodium sulfate and concentrated under reduced pressure. The crude brown oil was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119806B2
Source datasetuspto-grants-2012_02
ORD IDord-7f70f1c27bc1477b949291bd75e25437
Source noteuspto-grants-2012_02