HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1469190Generated: November 2, 2026
Methanol → (5-Bromo-2-chlorothiophen-3-yl)methanol
https://huagongshe.com/reaction/1469190
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | (Dimethyl sulfide)trihydroboron | HCID 12423031 | — |
| Reactant | 5-Bromo-2-chlorothiophene-3-carboxylic acid | HCID 22397190 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (5-Bromo-2-chlorothiophen-3-yl)methanol | HCID 23070160 | 99.3% |
Reaction Steps
To a solution of acid 1 (3.0 g, 12.4 mmol) in THF (50 mL) were added borane dimethylsulfide complex (10M in THF, 3.2 mL, 31.1 mmol) at 0° C. The mixture was stirred at 0° C. for 15 min, at room temperature for 45 min, and at 65° C. for 2 hours. The reaction mixture was cooled to 0° C. To the mixture were added MeOH (30 mL), H2O (250 mL) dropwise at 0° C. The mixture was extracted with EtOAc (100 mL). The organic layer was dried over MgSO4, filtered, and concentrated in vacuo to obtain the title compound 31 (2.8 g, 99%). The crude alcohol 31 was carried on to the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09006187B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-adf4f30a26f14787a65a0f0c1462f7b0 |
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| Source note | uspto-grants-2015_04 |
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