HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254190Generated: November 2, 2026
Methyl 4-(bromomethyl)-3-methoxybenzoate → HCID 19744376, compound
https://huagongshe.com/reaction/2254190
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 4-(bromomethyl)-3-methoxybenzoate | HCID 2759828 | — |
| Reactant | HCID 19744357 | HCID 19744357 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 19744376 | HCID 19744376 | 70% |
Reaction Steps
A mixture of 2.19 g. of sodium 3-chloro-6-nitroindazolide in 50 ml. methanol was stirred with 2.85 g methyl 3-methoxy-4-bromomethylbenzoate for 2 hours. After addition of 150 ml. water the resultant precipitate was collected and recrystallised from ethyl acetate to give methyl 4-[3-chloro-6-nitroindazol-1-yl-methyl]-3-methoxybenzoate in 70% yield as a solid, m.p. 167°-168° C. A mixture of 1.25 g. of this solid was hydrogenated in the presence of 385 mg. 5% w/w palladium on calcium carbonate in 20 ml. ethyl acetate and 20 ml. methanol for 3 hours at a pressure of 1.1 bar. The catalyst was removed by filtration through diatomaceous earth. The filtrate was concentrated to low volume in vacuo and the residue (ca 3 ml.) was diluted with ether and petroleum ether (b.p. 40°-60° C.) and cooled to -20° C. The precipitated solid was collected and dried at 80° C. to give the ester L in 90% yield, m.p. 131°-131.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05234942 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-3a1b2a247ca14535968df3444752b360 |
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| Source note | uspto-grants-1993_08 |
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