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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
Reactantethyl 3,4-dihydro-6-(phenylmethoxy)-2H-1-benzopyran-2-carboxylateHCID 20211052—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product3,4-dihydro-6-(phenylmethoxy)-2H-1-benzopyran-2-carboxaldehydeHCID 2021104697%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04654362
Source datasetuspto-grants-1987_03
ORD IDord-9457155e30764e7e8376ed3a5c2d4dd4
Source noteuspto-grants-1987_03