HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973283Generated: October 29, 2026
HCID 21493357, compound → HCID 21493363, compound
https://huagongshe.com/reaction/1973283
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 21493357 | HCID 21493357 | — |
| Reactant | HCID 21493360 | HCID 21493360 | — |
| Product | HCID 21493363 | HCID 21493363 | — |
Reaction Steps
A solution of 1,3-dihydro-1'-dimethylphosphinylmethyl-6-methoxy-3-phenylspiro[isobenzofuran-1,4'-piperidine] and 48% hydrobromic acid is heated under reflux, cooled, diluted with water, neutralized with sodium bicarbonate and extracted with chloroform. The chloroform solution is dried and the chloroform evaporated off, affording 1,3-dihydro-1'-dimethylphosphinylmethyl-6-hydroxy-3-phenylspiro[isobenzofuran-1,4'-piperidine]. In an analogous manner, 1,3-dihydro-1'-dimethylphosphinylmethyl-5-methoxy-3-phenylspiro[isobenzofuran-1,4'-piperidine] and 1,3-dihydro-1'-dimethylphosphinylmethyl-3-(4-methoxyphenyl)spiro[isobenzofuran-1,4'-piperidine] are treated to provide 1,3-dihydro-1'-dimethylphosphinylmethyl-5-hydroxy-3-phenylspiro[isobenzofuran-1,4'-piperidine] and 1,3-dimethylphosphinylmethyl-3-(4-hydroxyphenyl)spiro[isobenzofuran-1,4'-piperidine], respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03996354 |
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| Source dataset | uspto-grants-1976_12 |
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| ORD ID | ord-5a7c3477aa4f4913ad2ccf8e0310749d |
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| Source note | uspto-grants-1976_12 |
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