HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481817Generated: October 29, 2026
Hydrochloric Acid → HCID 19067324, compound
https://huagongshe.com/reaction/481817
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 6H-Dibenz[c,e][1,2]oxaphosphorin, 6-chloro- | HCID 89816 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Reactant | HCID 178489560 | HCID 178489560 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19067324 | HCID 19067324 | 98.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05789623 |
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| Source dataset | uspto-grants-1998_08 |
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| ORD ID | ord-d6bae647cf144f7ea83ed44f7c61ee34 |
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| Source note | uspto-grants-1998_08 |
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