HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701605Generated: October 27, 2026
Dimethylformamide → 3,4-Bis(pivalyloxy)phenyl tert-butylaminomethyl ketone
https://huagongshe.com/reaction/1701605
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | 1-(3,4-Dihydroxyphenyl)-2-((1,1-dimethylethyl)amino)ethan-1-one hydrochloride | HCID 3015704 | — |
| Reactant | Phenolate Sodium | HCID 4445035 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Product | 3,4-Bis(pivalyloxy)phenyl tert-butylaminomethyl ketone | HCID 12295036 | — |
Reaction Steps
Proceeding in a manner similar to that described in part A of Example 2 above, 17 g. of sodium methoxide was interacted with 26 g. of 3,4-dihydroxyphenyl tert-butylaminomethyl ketone hydrochloride in 200 ml. of N,N-dimethylformamide and the resulting sodium phenolate salt was interacted with 24 g. of pivalyl chloride (alternatively designated as trimethylacetyl chloride or 2,2-dimethylpropanoyl chloride). From this acylation reaction there was obtained 3,4-bis(pivalyloxy)phenyl tert-butylaminomethyl ketone which was treated with hydrochloric acid to yield 11.5 g. of 3,4-bis(pivalyloxy)phenyl tert-butylaminomethyl ketone hydrochloride as a white crystalline solid which melted at 243°-244° C. (dec.)(uncorr.). This salt was soluble in water at 25° C. to the extent of at least 1 percent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE030241 |
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| Source dataset | uspto-grants-1980_03 |
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| ORD ID | ord-cbde7ac3d5cc4312a65cd2cc9194ae88 |
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| Source note | uspto-grants-1980_03 |
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