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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479479Generated: November 1, 2026

Hydrochloric Acid → HCID 66874632, compound

https://huagongshe.com/reaction/1479479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrimethyl borateHCID 8470—
ReactantSodium HydroxideHCID 14798—
ReactantTert-butyl 2-fluorophenylcarbamateHCID 4935500—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 66874632HCID 66874632—

Reaction Conditions

Temperature-40 °C

Reaction Steps

To a solution of tert-butyl 2-fluorophenylcarbamate (from step 1) (1.0 eq.) in tetrahydrofuran (0.25 M) at −78° C. under N2 atmosphere was added dropwise 1.7 M tert-butyllithium (2.4 eq.). The reaction was warmed to −40° C. slowly over 2 hours, and neat trimethyl borate (3.8 eq.) was added. The reaction was warmed to room temperature over 30 minutes. An aqueous solution of 1N NaOH was slowly added to the reaction and stirred for 15 minutes. The mixture was poured into ethyl acetate and acidified with 3N HCl to dissolve the solids. The aqueous layer was extracted twice with ethyl acetate, and the combined organic layers were washed with brine, dried over anhydrous MgSO4, and concentrated en vacuo. The resulting solids were stirred in 1:1 ether/hexane, filtered, and dried. The solids were carried onto the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09408907B2
Source datasetuspto-grants-2016_08
ORD IDord-2674afcc9a284fe388ff3f237f729ead
Source noteuspto-grants-2016_08