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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481817Generated: October 29, 2026

Hydrochloric Acid → HCID 19067324, compound

https://huagongshe.com/reaction/481817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant6H-Dibenz[c,e][1,2]oxaphosphorin, 6-chloro-HCID 89816—
ReactantHCID 178418255HCID 178418255—
ReactantHCID 178489560HCID 178489560—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19067324HCID 1906732498.9%

Reaction Conditions

Temperature25 °C

Reaction Steps

23.5 g (100 mmol) of 6-chloro-6H-dibenz[c,e][1,2]oxa-phosphorine in 50 ml of anhydrous tetrahydrofuran are introduced, in an argon atmosphere with stirring, and a solution of 100 mmol of 2-methoxyphenylmagnesium bromide in tetrahydrofuran is added dropwise at -10° C. The mixture is slowly heated to 25° C. and stirred for 3 hours. A solution of 100 mmol of phenylmagnesium bromide in 150 ml of tetrahydrofuran is added dropwise and the mixture is then stirred for 5 hours at 65° C. The mixture is cooled to room temperature and 100 ml of water are added. The mixture is neutralized with dilute hydrochloric acid, the organic phase is separated off, dried with sodium sulfate and concentrated under reduced pressure. 38.0 g of colorless oil are obtained. By crystallization with methanol/water, 10:1, 32.7 g (86%) of colorless crystals having melting point 137° to 139° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05789623
Source datasetuspto-grants-1998_08
ORD IDord-d6bae647cf144f7ea83ed44f7c61ee34
Source noteuspto-grants-1998_08