HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481294Generated: November 2, 2026
Dichloromethane → HCID 18664242, compound
https://huagongshe.com/reaction/481294
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 13052472 | HCID 13052472 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 18664242 | HCID 18664242 | 33.4% |
Reaction Steps
A mixture comprising (4aR,8aS) isomer, (4aR,8aR) isomer and trans isomer of decahydroisoquinoline-3(S)-carboxylic acid was dissolved in 72 ml of water, followed by the addition of 60.9 g (725 mmol) of sodium hydrogencarbonate and 72 ml of dichloromethane at room temperature. Thereafter, 27.4 ml (290 mmol) of acetic anhydride was slowly dropwise added thereto, followed by stirring for 22 hours. Insolubles were separated by filtration. After 6N hydrochloric acid was poured thereinto to adjust to pH3, common salt was added thereto up to saturation. Extraction with chloroform was conducted and the organic layer was dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated in a reduced pressure. Dichloromethane was added thereto to thereby obtain 5.45 g of a crystal of the title compound. Yield 33.4% (two steps).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05789403 |
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| Source dataset | uspto-grants-1998_08 |
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| ORD ID | ord-683316f2e10644bbb37ae1b881bebb56 |
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| Source note | uspto-grants-1998_08 |
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