HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256045Generated: October 30, 2026
Sodium Chloride → HCID 20164963, compound
https://huagongshe.com/reaction/256045
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 20164914 | HCID 20164914 | — |
| Reactant | HCID 20164978 | HCID 20164978 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 20164963 | HCID 20164963 | — |
Reaction Steps
To a solution of a mixture of 803 g of t-butyl α-[6-amino-2-(1-naphthyl)-5-oxoperhydro-1,4-thiazepin-4-yl]acetate [prepared as described in step (g) above] and 1.13 g of ethyl 3-bromo-4-phenylbutyrate in 10 ml of dimethylformamide was added 0.66 g of sodium carbonate. The reaction mixture was stirred at 80° C. for 15 hours and then dissolved in a mixture of ethyl acetate and an aqueous solution of sodium chloride. The ethyl acetate layer was separated, washed with water and dried over anhydrous magnesium sulfate, and the solvent was then evaporated off. The residue was subjected to silica gel column chromatography using a 1:30 by volume mixture of ethyl acetate and methylene chloride as eluent, which separated the product into two isomers, A and B, (ascribed to the asymmetric carbon atom to which the phenethyl group is attached).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04699905 |
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| Source dataset | uspto-grants-1987_10 |
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| ORD ID | ord-e36f68f8969a4ea89556924241caa3a5 |
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| Source note | uspto-grants-1987_10 |
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