HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1082159Generated: October 31, 2026
Sodium Iodide → 3-(Tert-butyl-dimethylsilanyloxy)-2-formyl-5-methoxy-6-methyl-benzoic acid methyl ester
https://huagongshe.com/reaction/1082159
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 2-Formyl-3-hydroxy-5-methoxy-6-methylbenzoic acid methyl ester | HCID 53881817 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-(Tert-butyl-dimethylsilanyloxy)-2-formyl-5-methoxy-6-methyl-benzoic acid methyl ester | HCID 54444637 | 61.5% |
Reaction Steps
A mixture of 10.0 g of tert-butyl-dimethyl-chlorosilane and 10.0 g of sodium iodide in 50 ml of acetonitrile was stirred at room temperature for 1 h. The mixture was cooled to 0° C. and 14.0 g of 2-formyl-3-hydroxy-5-methoxy-6-methylbenzoic acid methyl ester were added at once followed by dropwise addition of 6.7 g of triethylamine over 15 min. The mixture was allowed to warm to room temperature and stirred for 2 h. The reaction mixture was partitioned between water and ethyl acetate. The organic layer was washed successively with 2N potassium hydrogensulfate, saturated sodium bicarbonate and brine, dried over magnesium sulfate and evaporated in vacuo. The solid residue was recrystallized from ethyl acetate/hexane to give 13.0 g of 3-(tert-butyl-dimethylsilanyloxy)-2-formyl-5-methoxy -6-methyl-benzoic acid methyl ester as white crystals, m.p: 125°-131° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05589473 |
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| Source dataset | uspto-grants-1996_12 |
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| ORD ID | ord-3a0123cb20214e31b21dd7e2dd502d92 |
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| Source note | uspto-grants-1996_12 |
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