HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6256Generated: October 26, 2026
Acetic Acid → (S)-1-Benzyloxy-3-(t-butyldiphenylsilyloxy)propan-2-ol
https://huagongshe.com/reaction/6256
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldiphenylchlorosilane | HCID 94078 | — |
| Reactant | (R)-3-(benzyloxy)propane-1,2-diol | HCID 2724795 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-1-Benzyloxy-3-(t-butyldiphenylsilyloxy)propan-2-ol | HCID 10982698 | 90% |
Reaction Steps
To a solution of (R)-3-benzyloxypropane-1,2-diol (prepared from (S)-4-benzylymethyl-2,2-dimethyl-1,3-dioxolane (commercially available from FLUKA) by acid hydrolysis using 80% aqueous acetic acid), (8.3 g, 47.2 mmol) in dry THF (70 ml) was added imidazole (6.42 g, 94.4 mmol). After 2 minutes, t-butyldiphenylsilyl chloride (12.28 ml, 47.2 mmol) was added. A white precipitate formed immediately. After 2 hours, the reaction mixture was filtered and the filtrate evaporated. The residue was partitioned between ethyl acetate and water, the organic layer separated, washed with saturated brine, dried (MgSO4), filtered and evaporated to give a colourless oil. Chromatography of the oil on silica gel (dichloromethane as eluant) afforded the title compound as a colourless oil (17.72 g, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05247085 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-cf9e57ba9a5d488b84ad34a0e5f55896 |
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| Source note | uspto-grants-1993_09 |
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