HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554764Generated: October 30, 2026
Ammonium Chloride → tert-butyl 4-(1-aminopropyl)benzoate Hydrochloride
https://huagongshe.com/reaction/554764
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Tert-butyl 4-formylbenzoate | HCID 2751588 | — |
| Reactant | Azane;hydrate | HCID 12896473 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | tert-butyl 4-(1-aminopropyl)benzoate Hydrochloride | HCID 66935393 | — |
Reaction Steps
To copper (I) iodide (3.1 g) in diethylether (70 ml) suspension, ethylmagnesium bromide (0.89M tetrahydrofuran solution) (35 ml) was added at −23° C. and the mixture was stirred at that temperature for 20 minutes. Next, tert-butyl 4-formylbenzoate (3 g) in diethylether (10 ml) solution was added to the reaction solution and the mixture was stirred at −23° C. for 30 minutes. Saturated ammonium chloride aqueous solution and 28% ammonia water were added to the reaction solution, the mixture was stirred at room temperature for 40 minutes, and the mixture was extracted with ethyl acetate. The organic layer was successively washed with distilled water and saturated saline, dried over with anhydrous sodium sulfate, then concentrated. The obtained compound (3.7 g) was used as an starting material instead of the starting material of Reference Example 83, that is, the compound S82, while 4N hydrochloric acid/ethyl acetate was used instead of L-tartaric acid for the similar procedure as in Reference Example 83 to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08049006B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-66faf4ca8be445c3a1860737a7e4c5d8 |
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| Source note | uspto-grants-2011_11 |
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