HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444058Generated: November 1, 2026
Ethyl 5-bromovalerate → HCID 22815604, compound
https://huagongshe.com/reaction/444058
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 5-bromovalerate | HCID 84580 | — |
| Reactant | Ethyl cysteinate hydrochloride | HCID 2723617 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Monosodium phosphate | HCID 23672064 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22815604 | HCID 22815604 | — |
Reaction Steps
L-Cysteine ethyl ester hydrochloride (18.6 g; 0.10 mole) was added to a solution of sodium (4.6 g; 0.20 g.a) in ethanol (320 ml, absolute), stirred 15 minutes and then the solvent removed in vacuo. To a solution of the residual sodium salts in dry dimethylsulphoxide (200 ml) was added ethyl 5-bromovalerate (21.0 g; 0.10 mole) in a single portion with stirring. The reaction mixture was allowed to stand at room temperature overnight, warmed on a steam bath for 5 mins. and then poured onto water (300 ml) containing sodium dihydrogen phosphate (1 g). The oil was extracted with ether (3×), the combined extracts washed with water and dried over MgSO4. The solvent was removed in vacuo yielding the product as a pale yellow oil which was used in Example 70.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04262128 |
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| Source dataset | uspto-grants-1981_04 |
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| ORD ID | ord-f4c9c5c8433547e8964623eafb90fb57 |
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| Source note | uspto-grants-1981_04 |
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