HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075363Generated: October 26, 2026
Thionyl Chloride → 3,5-Di-t-butylbenzoyl chloride
https://huagongshe.com/reaction/1075363
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3,5-Bis(tert-butyl)benzoic acid | HCID 85339 | — |
| Product | 3,5-Di-t-butylbenzoyl chloride | HCID 11817622 | — |
Reaction Steps
This compound was prepared by chlorination of 3,5-di-t-butylbenzoic acid with thionyl chloride using standard procedures to give 3,5-di-t-butylbenzoyl chloride. 3.26 g (12.9 mmol) of the chloride was then reacted with 1.95 g (16.8 mmol) of N,N-diethylethylenediamine in dry chloroform. The reaction mixture was concentrated by evaporation of chloroform and treated with sodium bicarbonate in a mixture of ethanol and water. Following extraction with chloroform, the combined chloroform extracts were dried and concentrated, upon which the amide began to crystallize. Without further purification, the amide was reduced with lithium aluminum hydride in THF using standard procedures. After quenching and filtration of the reaction mixture, the filtrate was dried and concentrated then distilled under reduced pressure to yield 2.00 g (49%) of the diamine.(bp 105-108°, 10 v). Purity by GC>99%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05900213 |
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| Source dataset | uspto-grants-1999_05 |
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| ORD ID | ord-1cadae05e71841049acca791fddc8561 |
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| Source note | uspto-grants-1999_05 |
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