HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906900Generated: October 31, 2026
Hydrochloric Acid → 3,4-dihydro-6-(phenylmethoxy)-2H-1-benzopyran-2-carboxaldehyde
https://huagongshe.com/reaction/1906900
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | ethyl 3,4-dihydro-6-(phenylmethoxy)-2H-1-benzopyran-2-carboxylate | HCID 20211052 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3,4-dihydro-6-(phenylmethoxy)-2H-1-benzopyran-2-carboxaldehyde | HCID 20211046 | 97% |
Reaction Steps
To a stirred solution of 48 parts of ethyl 3,4-dihydro-6-(phenylmethoxy)-2H-1-benzopyran-2-carboxylate in 495 parts of methylbenzene were added dropwise 108 parts of a solution of [bis(2-methylpropyl)]aluminium hydride in methylbenzene at -80° C. Upon completion, stirring was continued for 30 minutes at -80° C. The reaction mixture was decomposed by the carefully addition of 24 parts of methanol. It was poured into 1000 parts of water and the whole was stirred for 15 minutes very carefully! The mixture was acidified with concentrate hydrochloric acid. After stirring for 5 minutes, the organic layer was separated, washed with water, dried, filtered and evaporated, yielding 39.8 parts (97%) of 3,4-dihydro-6-(phenylmethoxy)-2H-1-benzopyran-2-carboxaldehyde as a residue (intermediate 42).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04654362 |
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| Source dataset | uspto-grants-1987_03 |
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| ORD ID | ord-9457155e30764e7e8376ed3a5c2d4dd4 |
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| Source note | uspto-grants-1987_03 |
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