HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052166Generated: October 29, 2026
Triethylamine → Propanoic acid, 2,2-dimethyl-, (((4-((4-chlorophenyl)methyl)phenoxy)acetyl)oxy)methyl ester
https://huagongshe.com/reaction/2052166
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acetic acid, 2-(4-(4-chlorobenzyl)phenoxy)- | HCID 42121 | — |
| Reactant | Chloromethyl pivalate | HCID 87885 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Propanoic acid, 2,2-dimethyl-, (((4-((4-chlorophenyl)methyl)phenoxy)acetyl)oxy)methyl ester | HCID 3044347 | — |
Reaction Steps
To a solution of 8.3 g (0.06 mol) of 4-(4'-chlorobenzyl)-phenoxy acetic acid in 50 ml of dimethylformamide are added 6.0 g (0.06 mol) of triethylamine, whereafter the mixture is stirred for 30 minutes at room temperature and, after adding 9.0 g (0.06 mol) of chloromethyl pivalate, is heated for 6 hours in an oil bath at 85°-90° C. The residue which is obtained by concentration by evaporation at reduced pressure in a Buchi rotary evaporator is washed with water and extracted with ether. The ethereal solution is once again washed with water, dried over anhydrous magnesium sulphate and concentrated by evaporation in the Buchi rotary evaporator, an oil being obtained which quickly solidifies. By recrystallisation from ether/n-hexane, 9.5 g of product are obtained in the form of white crystals with the melting point 54°-55° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04182902 |
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| Source dataset | uspto-grants-1980_01 |
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| ORD ID | ord-353e7cf9f2524da7ad03f0ff8e783043 |
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| Source note | uspto-grants-1980_01 |
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