HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865458Generated: October 30, 2026
2,4-Dichlorobenzoyl chloride → 2,4-Dichloro-N-[(8-cyclopropylmethyl-1,4-dioxaspiro[4.5]dec-8-yl)methyl]benzamide
https://huagongshe.com/reaction/1865458
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4-Dichlorobenzoyl chloride | HCID 66645 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 8-(Cyclopropylmethyl)-1,4-dioxaspiro[4.5]decane-8-methanamine | HCID 68683620 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,4-Dichloro-N-[(8-cyclopropylmethyl-1,4-dioxaspiro[4.5]dec-8-yl)methyl]benzamide | HCID 68682473 | — |
Reaction Steps
To a solution of {[8-(cyclopropylmethyl)-1,4-dioxaspiro[4.5]dec-8-yl]methyl}amine (7 g; 31.0 mmol) and n-ethyldiisopropylamine (6.45 ml; 37.2 mmol) in DCM (60 ml) at 0° C. was added 2,4-dichlorobenzoyl chloride (4.781 ml; 34.17 mmol) dropwise and the solution stirred for 4 hours warming to ambient temperature. The reaction was partitioned between DCM (50 ml) and water (20 ml). The aqueous phase was extracted with DCM (20 ml) and the combined organics dried over MgSO4, filtered and evaporated to give a colourless oil which was used in the next step without further purification. (11.5 g) 1H NMR δ (ppm)(CDCl3): 7.67 (1H, d, J=8.3 Hz), 7.43 (1H, d, J=2.0 Hz), 7.32 (1H, dd, J=2.0, 8.4 Hz), 6.25 (1H, s), 3.93 (4H, s), 3.56 (2H, d, J=6.2 Hz), 1.67 (8H, m)), 1.33 (2H, d, J=6.7 Hz), 0.75-0.65 (1H, m), 0.51-0.47 (2H, m), 0.05 (2H, q, J=5.0 Hz). MS (m/e)=398
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07626056B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-7bedd9be41a641fcb2b5dbbf162aed90 |
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| Source note | uspto-grants-2009_12 |
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