Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 4-Bromoanisole | HCID 7730 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 19377743 | HCID 19377743 | — |
| Product | HCID 178491912 | HCID 178491912 | — |
Reaction Steps
A solution of p-methoxyphenyl magnesium bromide was prepared from p-bromo-anisole (18.5 g) and magnesium (2.5 g)in tetrahydrofuran (50 ml). The solution was cooled to -40° to -50° C. and methylene chloride (25 ml) was added followed by a solution of 7-chloro- 1,2,3,4,4a,9b-hexahydro-2-methyl-5H-1,3-ethanoindeno-[1,2-c]pyridin-5-one (9.16 g) (compound (2))in methylene chloride (40 ml). The solution was stirred first at -50° C. then overnight at 0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05461057 |
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| Source dataset | uspto-grants-1995_10 |
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| ORD ID | ord-4d71f24b5fe74135a8a5ae0750e6585a |
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| Source note | uspto-grants-1995_10 |
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