HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647543Generated: October 31, 2026
Phenyl chloroformate → HCID 12694090, compound
https://huagongshe.com/reaction/647543
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | HCID 12694071 | HCID 12694071 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 12694090 | HCID 12694090 | — |
Reaction Steps
To 5.0 g of phenyl chloroformate in 80 ml of dichloromethane is added 7.89 g of the free base, 3-(3-fluorophenyl)-1,3-dihydro-1'-methylspiro[benzo(c)thiophene-1,4'-piperidine] of Example 55, in 10 ml of dichloromethane over 20 minutes. The reaction mixture is stirred at room temperature for 21 hours, then diluted with 200 ml of dichloromethane. The resultant mixture is washed with two 175 ml portions of 10% aqueous sodium hydroxide solution, two 150 ml portions of water and one 70 ml portion of saturated aqueous sodium chloride solution, and dried over magnesium sulfate to give an oil. The oil is chromatographed on silica gel with dichloromethane to give an oil, which crystallizes to yield 3-(3-fluorophenyl)-1,3-dihydro-1'-phenoxycarbonylspiro[benzo(c)thiophene-1,4'-piperidine], m.p. 134°-142° C. A portion is recrystallized twice from toluene:hexane, m.p. 144°-146° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04409229 |
|---|
| Source dataset | uspto-grants-1983_10 |
|---|
| ORD ID | ord-1a78b598fd4c4979b5159e292dc6f6b3 |
|---|
| Source note | uspto-grants-1983_10 |
|---|