HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328864Generated: October 29, 2026
(+/-)-Methyl 6-benzyloxy-2,5,7,8-tetramethylchroman-2-acetate → (6-Benzyloxy-2,5,7,8-tetramethylchroman-2-yl)acetaldehyde
https://huagongshe.com/reaction/328864
Participants
| Role | Name | HCID | Charge |
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| Reactant | (+/-)-Methyl 6-benzyloxy-2,5,7,8-tetramethylchroman-2-acetate | HCID 14368720 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Pentane | HCID 8003 | — |
| Product | (6-Benzyloxy-2,5,7,8-tetramethylchroman-2-yl)acetaldehyde | HCID 13422213 | — |
Reaction Steps
A solution of 31.17 g. of (±)-methyl 6-benzyloxy-2,5,7,8-tetramethylchroman-2-acetate in 3.11. of pentane was cooled under N2 to -70° Diisobutylaluminum hydride (24.4% in toluene; 87.3 ml.) in 87 ml. of pentane was added over 14 minutes. After 1.0 hour at -70°, another 8.73 ml. of diisobutylaluminum hydride was added and stirring was continued and additional 0.25 hour. The reaction was quenched by the careful addition of 250 ml. of methanol at -70°. The mixture was diluted with 1.01. of ether, washed with 0.5 N HCl, H2O, and brine and dried over sodium sulfate. Solvent removal gave a light yellow oil, which was filtered through 500 g. of silica gel with 90:10 benzene-ethyl acetate. Crystallization of the resulting oil from hexane - 30°-60° petroleum ether gave (±) 6-benzyloxy-2,5,7,8-tetramethylchroman- 2-acetaldehyde as a white solid, m.p. 70°-75° .
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04018799 |
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| Source dataset | uspto-grants-1977_04 |
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| ORD ID | ord-7b048f9701ee43dea0df49ea0543646d |
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| Source note | uspto-grants-1977_04 |
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