HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224294Generated: October 30, 2026
Dimethylformamide → 3-Formyl-1-(p-hydroxyphenyl)-3-azabicyclo[3.1.0]hexane
https://huagongshe.com/reaction/224294
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(4-Methoxyphenyl)-3-azabicyclo[3.1.0]hexane Hydrochloride | HCID 12719856 | — |
| Product | 3-Formyl-1-(p-hydroxyphenyl)-3-azabicyclo[3.1.0]hexane | HCID 12719876 | — |
Reaction Steps
To a slurry of 7.2 g (0.15 mol) of sodium hydride (50% oil dispersion) in 170 ml of N,N-dimethylformamide at 0°-5° is added a solution of 10.1 ml of ethanethiol in 85 ml of N,N-dimethylformamide over a 15 minute period. An additional 3.16 g portion of sodium hydride is added followed by 14.4 g of 1-(p-methoxyphenyl)-3-azabicyclo[3.1.0]hexane hydrochloride. After the addition of 40 ml of N,N-dimethylformamide, the mixture is refluxed for 4 hours and the solvent is then removed. The residue is dissolved in 150 ml of water and mineral oil is extracted with ether. The aqueous solution is made acidic with acetic acid and the precipitated crystals are collected by filtration to give 9.8 g of 3-formyl-1-(p-hydroxyphenyl)-3-azabicyclo[3.1.0]hexane as tan crystals, m.p. 166°-167°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04231935 |
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| Source dataset | uspto-grants-1980_11 |
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| ORD ID | ord-25d4771394784761838de129e42cf2eb |
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| Source note | uspto-grants-1980_11 |
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