HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979959Generated: November 1, 2026
Hydrochloric Acid → HCID 178447591, compound
https://huagongshe.com/reaction/1979959
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Chloromethyl pivalate | HCID 87885 | — |
| Reactant | Sodium Bromide | HCID 253881 | — |
| Reactant | HCID 178453624 | HCID 178453624 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178447591 | HCID 178447591 | — |
Reaction Steps
Chloromethyl pivalate (33.2 g; 0.22 mol) was added to a suspension of sodium bromide (22.4 g; 0,22 mol) in dimethylformamide. After 2 h a solution of trans-4-(tert.-butyloxycarbonylaminomethyl)cyclohexanecarboxylic acid in triethylamine (24 g; 0.24 mol) and dimethylformamide was added. The mixture was stirred overnight at room temperature. The solvent was distilled off and water (1 L) and dichloromethane was added. The organic layer was separated, washed, dried and evaporated to yield 55 g. This product was dissolved in ethyl acetate and cooled. A solution of hydrochloric acid in ethyl acetate was added. After 1 h ether was added. The precipitate was filtered, washed and dried to yield 30.2 g, m.p. 165° C. after crystallisation from acetone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04483867 |
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| Source dataset | uspto-grants-1984_11 |
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| ORD ID | ord-516bd06c75b64118a08de82a2ad0ba85 |
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| Source note | uspto-grants-1984_11 |
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