HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762174Generated: October 26, 2026
4-tert-Butylbenzoic acid → Methyl 4-[2-(4-tert-butylbenzamido)ethoxy]benzoate
https://huagongshe.com/reaction/1762174
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-tert-Butylbenzoic acid | HCID 7403 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Methyl 4-(2-aminoethoxy)benzoate | HCID 14097616 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Methyl 4-[2-(4-tert-butylbenzamido)ethoxy]benzoate | HCID 14426625 | 91.9% |
Reaction Steps
p-tert-Butylbenzoic acid (5.35 g) and 3.34 g of triethylamine were dissolved in 70 ml of chloroform and 3.26 g of ethyl chloroformate was dropped into the above mixture with stirring and cooling at 0° to 5° C. After the dropping, the mixture was stirred at the same temperature for 30 minutes and, after addition of 5.86 g of methyl 4-(2-aminoethoxy)benzoate thereto, the mixture was stirred for 6 hours more. The reaction solution was washed with 10% hydrochloric acid, saturated potassium carbonate solution, and water, dried with anhydrous magnesium sulpahte, concentrated in vacuo, and the residue was crystallised with n-hexane to give 9.8 g of crystals which were further recrystallised from ethyl acetate to give 7.64 g (yield: 71.65%) of the product, m.p. 112°-114° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04831055 |
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| Source dataset | uspto-grants-1989_05 |
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| ORD ID | ord-7c50a48fc6d84b4197668e9e297aa4e0 |
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| Source note | uspto-grants-1989_05 |
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