HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479384Generated: October 30, 2026
Hydrochloric Acid → HCID 18770431, compound
https://huagongshe.com/reaction/479384
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 18770408 | HCID 18770408 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 18770431 | HCID 18770431 | 99.7% |
Reaction Steps
An aqueous 5N sodium hydroxide (5 ml; 25 mmol) was added to a solution in methanol (5 ml) of methyl 2,2-bis[(1-tert-butoxycarbonyl-4-piperidinyl)methyl]acetate (906 mg; 1.9 mmol) synthesized by the process described in Referential Example 3, and the mixture was stirred for 30 minutes in a bath controlled at 100° C. The reaction mixture was made acidic by addition of 6N hydrochloric acid and extracted with chloroform. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The resultant crude oil was purified by column chromatography on silica gel, thereby obtaining 861 mg (yield: 98%) of 2,2-bis[(1-tert-butoxycarbonyl-4-piperidinyl)methyl]acetic acid as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06645957B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-5e6b0a1e4d98465e9d3f41b541ef13fd |
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| Source note | uspto-grants-2003_11 |
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