HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964971Generated: October 27, 2026
Morpholine → 2-cyclopropyl-7,8-dimethoxy-2H-chromene-5-carbaldehyde
https://huagongshe.com/reaction/964971
Participants
| Role | Name | HCID | Charge |
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| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Cyclopropyl-7,8-dimethoxy-2H-chromene-5-carboxylic acid methyl ester | HCID 11644974 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-cyclopropyl-7,8-dimethoxy-2H-chromene-5-carbaldehyde | HCID 11550670 | — |
Reaction Steps
A solution of 48 ml of morpholine in 50 ml of toluene was added dropwise over 1 hr. under argon to an ice-cold solution of 143 ml of sodium dihydrido-bis-(2-methoxyethoxy) aluminate (3.5M in toluene) diluted with 200 ml of toluene. The resulting reduction solution was then added dropwise under argon during 1 hr. to a solution, cooled to -35° C., of 46 g of methyl (RS)-2-cyclopropyl-7,8-dimethoxy-2H-1-benzopyran-5-carboxylate in 200 ml of toluene and the mixture was stirred at -15° C. for a further 4 hrs. The reaction was stopped by the cautious addition of 40 ml of 3N NaOH and the mixture was left to warm. Extraction: 3×600 ml of ice-water, 1×600 ml of toluene. Chromatography: silica gel, hexane/ethyl acetate 5:1. Crystallization from diethyl ether/ hexane. (RS)-2-Cyclopropyl-7,8-dimethoxy-2H-1-benzopyran-5-carbaldehyde was obtained as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05773446 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-c32069861fe143aaab9eebead4e96932 |
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| Source note | uspto-grants-1998_06 |
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