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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889784Generated: October 30, 2026

Hydrochloric Acid → HCID 59582968, compound

https://huagongshe.com/reaction/889784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantTriisopropyl borateHCID 21531—
ReactantHCID 14415981HCID 14415981—
ReactantHCID 178418244HCID 178418244—
ProductHCID 59582968HCID 5958296860%

Reaction Conditions

Temperature-40 °C

Reaction Steps

Under an argon atmosphere, 5.87 g of 10-bromobenzo[g]chrysene which had been prepared in Synthesis Example 2 was placed in a flask and 100 mL of dehydrated ether was added to this flask. The reaction solution was cooled to −40° C. and 11 ml of 1.6M n-butyllithium hexane solution was added. After heating to 0° C., the resultant was stirred for 1 hour. The reaction solution was cooled to −60° C. and 10 mL of dehydrated ether solution in which 7.72 g of triisopropyl borate was dissolved was added. The reaction solution was stirred for 5 hours with heating to room temperature. 50 mL of 10% aqueous solution of hydrochloric acid was added and stirring was conducted for 1 hour. An aqueous phase was removed and an organic phase which had been separated was washed with water and saturated brine, and then dried with magnesium sulfate. After the magnesium sulfate was filtered out, the organic phase was concentrated. The resulting solids were washed with hexane, whereby 3.18 g (yield: 60%) of benzo[g]chrysene-10-boronic acid was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08253129B2
Source datasetuspto-grants-2012_08
ORD IDord-8b4ba2cd6f0f411f8ae6c96eb7c21df9
Source noteuspto-grants-2012_08