HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616588Generated: November 1, 2026
Bromomethyl 2-methoxyphenyl ketone → HCID 59167790, compound
https://huagongshe.com/reaction/1616588
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromomethyl 2-methoxyphenyl ketone | HCID 123440 | — |
| Reactant | HCID 23254886 | HCID 23254886 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59167790 | HCID 59167790 | 142.4% |
Reaction Steps
Add THF (125 mL, anhydrous) to a sealed vessel containing 5-thiocarbamoyl-pentanoic acid methyl ester (7.25 g, 41.4 mmol) and 2-bromo-2′-methoxyacetophenone (9.48 g, 41.4 mmol). Flush vessel with N2, seal, and heat at 80° C. overnight. Cool to room temperature, add EtOAc, wash with saturated aqueous NaHCO3 solution, brine, and backextract from each aqueous layer with EtOAc. Dry combined organic layers over MgSO4 and concentrate to get 18 grams of purple residue. Adsorb on SiO2 and purify the residue by flash chromatography on silica gel eluting with 0-20% EtOAc/hexanes to afford the title compound (9.7 g, 77%). TLC (30% EtOAc/hexanes) Rf=0.38. MS (IS) 306 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08765796B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-c332ca81a1e34d91b68d9bc5be1ecc7a |
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| Source note | uspto-grants-2014_07 |
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