HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390901Generated: October 31, 2026
Sulfuric Acid → rac. 4-Benzyloxy-3-methylbutanal
https://huagongshe.com/reaction/1390901
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-(Benzyloxy)-3-methylbutanenitrile | HCID 10976273 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | rac. 4-Benzyloxy-3-methylbutanal | HCID 14658350 | — |
Reaction Steps
A solution of 5.8 g. (0.0307 mole) of rac. 4-benzyloxy-3-methylbutyronitrile in 290 ml. of hexane was stirred at -65° C. to -70° C. while 22.4 ml. (4.78 g.; 0.0337 mole) of 25% diisobutylaluminum hydride solution in toluene was added dropwise. The resulting solution was stirred at -65° C. to -70° C. for 0.5 hours then at room temperature for 5 hours whereupon 2.8 ml. of ethyl formate was added dropwise. The reaction mixture was then treated with 250 ml. of saturated aqueous ammonium chloride solution. Stirring was continued for 20 minutes at which point 125 ml. of 5% by weight aqueous sulfuric acid was added and stirring was continued for an additional 10 minutes. The organic layer was separated and the aqueous layer was extracted with ether. The organic solutions were combined and processed as in Example 1 giving 4.79 g. (81.3%) of rac. 4-benzyloxy-3-methylbutanal as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04140723 |
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| Source dataset | uspto-grants-1979_02 |
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| ORD ID | ord-9bb9c4a4d7b2432c99f0fdd6c31d255c |
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| Source note | uspto-grants-1979_02 |
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