HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Chloride → Ethyl 2-[(6-chloronaphthalen-2-ylsulfonyl)(2,2-diethoxyethyl)amino]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 6-Chloronaphthalene-2-sulfonyl chloride | HCID 10635129 | — |
| Reactant | Ethyl 2-[(2,2-diethoxyethyl)amino]acetate | HCID 11790686 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-[(6-chloronaphthalen-2-ylsulfonyl)(2,2-diethoxyethyl)amino]acetate | HCID 11812307 | 73.5% |
Reaction Steps
The compound obtained in Step 1 (504 mg) was suspended in methylene chloride (20 ml) and to the suspension were added triethylamine (336 ml) and then 6-chloronaphthalene-2-sulfonyl chloride (600 mg) under cooling with ice. After stirring the mixture overnight at room temperature, saturated sodium chloride solution was added and the mixture was extracted with methylene chloride. The organic layer was dried over anhydrous sodium sulfate and thereafter the solvent was distilled off under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent; n-hexane:ethyl acetate=20:1–4:1) to obtain the title compound (750 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07122662B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-250da0f4600049208aeaaa79bda6e47c |
| Source note | uspto-grants-2006_10 |