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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 886949Generated: October 29, 2026

Carbon Dioxide → 1055880-94-8

https://huagongshe.com/reaction/886949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantHydrochloric AcidHCID 313—
ReactantHexaneHCID 8058—
ReactantAmmonium ChlorideHCID 25517—
ReactantTert-butyl 9-bromo-2,3-dihydrobenzo[F][1,4]oxazepine-4(5H)-carboxylateHCID 59403519—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1055880-94-8HCID 6857811222.6%

Reaction Conditions

Temperature78 °C

Reaction Steps

To a solution of tert-butyl 9-bromo-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylate (200 mg, 0.605 mmol) in tetrahydrofuran (4 ml) was added 1.6N solution of n-butyllithium in hexane (0.396 ml, 0.634 mmol) at −78° C., and the mixture was stirred at 78° C. for 1 hr. At −78° C., pulverized dry ice (2 g) was added to the reaction mixture, and the mixture was stirred for 1 hr. Saturated aqueous ammonium chloride solution (5 ml) and 1N hydrochloric acid (5 ml) were added, and the mixture was extracted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate) to give the desired product (40.0 mg, 22.6%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247403B2
Source datasetuspto-grants-2012_08
ORD IDord-3faaabdc62ce4dc6820cea03a9b54c38
Source noteuspto-grants-2012_08