HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289094Generated: October 30, 2026
2,2-Dibromopropane → HCID 21251132, compound
https://huagongshe.com/reaction/2289094
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2-Dibromopropane | HCID 11658 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 15840683 | HCID 15840683 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21251132 | HCID 21251132 | — |
Reaction Steps
A solution of 3-chloro-4-dimethylcarbamoylthiophenyl acetic acid methyl ester (10.028 grams; 34.848 mmol) in dry MeOH (90 mL) was treated with a solution of sodium methoxide (4.37 M; 11.16 mL; 48.788 mmol). The reaction was refluxed for 2 hours. The reaction mixture was cooled to 20 ° C. and transferred to a dropping funnel. The dropping funnel was placed atop a flask containing a solution of dibromopropane (14.15 mL; 139.392 mmol) in dry MeOH (50 mL). The contents of the dropping funnel were added to the flask dropwise, and the solution stirred for 2 hours. The reaction mixture was partitioned between isopropyl acetate and pH 4 buffer. The layers were separated and the organic washed once with water. The organic was dried over magnesium sulfate, filtered and concentrated. Silica gel chromatography afforded 3-chloro-4-(3-bromopropyl)thiophenyl acetic acid methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06090836 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-2955abd08e204ba9b132028855d0f81b |
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| Source note | uspto-grants-2000_07 |
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