HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1935402Generated: October 31, 2026
Chloroacetyl chloride → HCID 10594703, compound
https://huagongshe.com/reaction/1935402
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Carbamic acid, [(1S)-1-[[(2,3-dimethylphenyl)amino]methyl]pentyl]-, 1,1-dimethylethyl ester | HCID 10615682 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 10594703 | HCID 10594703 | — |
Reaction Steps
A solution of the product from Step C (8.50 g, 26.5 mmol) in ethyl acetate (250 mL) was vigorously stirred at 0° C. with saturated sodium bicarbonate (150 mL). Chloroacetyl chloride (2.33 mL, 29.1 mmol) was added, and the reaction stirred at ) 0° C. for 1 h. The layers were separated, and the ethyl acetate phase was washed with saturated brine, and dried over magnesium sulfate. The crude product was dissolved in DMF (300 mL) and cooled to 0° C. under nitrogen. Sodium hydride (1.79 g, 60% dispersion in oil, 44.9 mmol) was added portionwise to maintain moderate hydrogen evolution. After 30 min, an additional amount of sodium hydride was added (0.8 g). The reaction was stirred another 30 min, then quenched with saturated ammonium chloride. The DMF was distilled in vacuo, and the residue partitioned between ethyl acetate and water. The organic phase was washed with water, saturated brine, and dried over magnesium sulfate. The crude product was chromatographed on silica gel with 20-30% ethyl acetate in hexane to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06387903B1 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-2e9ab6661d604040824b5a45d7ed4621 |
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| Source note | uspto-grants-2002_05 |
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