HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → Ethyl 4-carbamoyloxy-4-methyl-2-pentynoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | 4-Hydroxy-4-methyl-pent-2-ynoic acid ethyl ester | HCID 11228926 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 4-carbamoyloxy-4-methyl-2-pentynoate | HCID 13343299 | 33.6% |
Reaction Steps
To 100 ml of a dichloromethane solution containing 4.9 g (31.4 millimoles) of ethyl 4-hydroxy-4-methyl-2-pentynoate, 3 ml (34.5 millimoles) of chlorosulfonyl isocyanate was added at a temperature of -10° C. The mixture was reacted for 30 minutes at -10° C. under stirring. The reaction mixture was returned to room temperature, and 20 ml of water was added thereto. The mixture was stirred for 15 minutes for hydrolysis treatment. The dichloromethane phase was separated by phase separation, washed with a 10% barium chloride solution and water successively, dried over sodium sulfate and then concentrated under reduced pressure, whereby 2.1 g (yield: 33%) of ethyl 4-carbamoyloxy-4-methyl-2-pentynoate in crystal form was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04914227 |
| Source dataset | uspto-grants-1990_04 |
| ORD ID | ord-3a55dd24c1c2464496b5473514b0bdca |
| Source note | uspto-grants-1990_04 |