HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428175Generated: October 29, 2026
Acetic Anhydride → n-[2-(3,4-Dihydro-2h-4-chromenyl)ethyl]acetamide
https://huagongshe.com/reaction/428175
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2-(Chroman-4-yl)acetonitrile | HCID 13362781 | — |
| Catalyst | Nickel | HCID 935 | — |
| Product | n-[2-(3,4-Dihydro-2h-4-chromenyl)ethyl]acetamide | HCID 18177447 | — |
Reaction Steps
The saturated cyano compound obtained in Step B is solubilized in the reactor of a Parr apparatus with acetic anhydride. Sodium acetate (1.5 eq.) and also Raney nickel (6 mg per 50 mg of product) are then introduced into the reaction medium. The whole is heated at 50° C. under hydrogen pressure of 40 psi for 12 hours. Once the solvent has been removed after returning to normal temperature and pressure conditions, extraction is carried out with ethyl acetate. Purification of the concentrated organic phase by flash chromatography (CHCl3/AcOEt 7/3) results in the desired amide. Colourless gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06313160B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-c82db8a0e861465ab0d824918a33f986 |
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| Source note | uspto-grants-2001_11 |
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