HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921874Generated: October 26, 2026
Hydrochloric Acid → 1,3-Difluoro-5-hydroxymethyl-2-triisopropylsilanyloxybenzene
https://huagongshe.com/reaction/1921874
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3,5-Difluoro-4-triisopropylsilanyloxybenzaldehyde | HCID 57971920 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1,3-Difluoro-5-hydroxymethyl-2-triisopropylsilanyloxybenzene | HCID 57971896 | — |
Reaction Steps
35.0 g (111 mmol) of 3,5-difluoro-4-triisopropylsilanyloxybenzaldehyde are introduced into 150 ml of water and 40 ml of methanol, cooled to 0° C. and, after addition of 8.42 g (222 mmol) of sodium borohydride in portions, stirred at RT overnight. The mixture is cautiously acidified with 1 N hydrochloric acid and extracted with ethyl acetate, and the combined organic phases are washed with saturated sodium chloride solution and dried over magnesium sulfate, and the solvent is distilled out in vacuo. Chromatography on silica gel 60 (mobile phase: cyclohexane/ethyl acetate 4:1) results in 29.5 g (93.2 mmol, 84% of theory) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08173704B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-74494ef89d704db8a97c6cb4d099dcd0 |
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| Source note | uspto-grants-2012_05 |
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