HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279485Generated: October 30, 2026
Hydrochloric Acid → (αS)-3,4-Dichloro-α-ethylbenzenemethanol
https://huagongshe.com/reaction/2279485
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethylaniline-borane | HCID 83312 | — |
| Reactant | 1-(3,4-Dichlorophenyl)-1-propanone | HCID 599598 | — |
| Reactant | (R)-2-Methyl-CBS-oxazaborolidine | HCID 9838490 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | (αS)-3,4-Dichloro-α-ethylbenzenemethanol | HCID 25665794 | 67% |
Reaction Steps
A 250 mL round-bottom flask was charged with MTBE (35 mL), a solution of (R)-1-methyl-3,3-diphenylhexahydropyrrolo[1,2-c][1,3,2]oxazaborole (2.51 mL, 2.51 mmol) and borane diethylaniline (4.45 mL, 25.1 mmol) at RT then heated to 40° C. A MTBE (20 mL) solution of 156 (6.00 g, 25.1 mmol) was added dropwise and the reaction was stirred at 40° C. for 3 h. The reaction was cooled to RT and MeOH (5 mL) was then added slowly, followed by 1M HCl and the reaction was stirred for 18 h. The water was removed and the remaining organic phase dried (Na2SO4), filtered and concentrated to get a light gray oil. The crude product was purified by SiO2 chromatography (SNAP 100) eluting with EtOAc/hexane (1:3) to afford 3.45 g (66%) of (S)-1-(3,4-dichlorophenyl)propan-1-ol (158) as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133187B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-67d66dd55314418ca516d09110611aff |
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| Source note | uspto-grants-2015_09 |
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