HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502844Generated: October 27, 2026
Dimethylformamide → (2-Bromo-5-iodophenyl)methanol
https://huagongshe.com/reaction/502844
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-Bromo-5-iodobenzoic acid | HCID 2735572 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2-Bromo-5-iodophenyl)methanol | HCID 53424372 | — |
Reaction Steps
Oxalyl chloride (13.0 mL) is added to an ice-cold solution of 2-bromo-5-iodo-benzoic acid in CH2Cl2 (200 mL). DMF (0.2 mL) is added and the solution is stirred at room temperature for 6 h. Then, the solution is concentrated under reduced pressure and the residue is dissolved in THF (100 mL). The resulting solution is cooled in an ice-bath and LiBH4 (3.4 g) is added in portions. The cooling bath is removed and the mixture is stirred at room temperature for 1 h. The reaction mixture is diluted with THF and treated with 0.1 M hydrochloric acid. Then, the organic layer is separated and the aqueous layer is extracted with ethyl acetate. The combined organic layers are dried (Na2SO4) and the solvent is evaporated under reduced pressure to give the crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07776830B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-5d971f84d0ad41338b8b27629245dd72 |
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| Source note | uspto-grants-2010_08 |
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