HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25591Generated: October 26, 2026
Hydrochloric Acid → HCID 178486042, compound
https://huagongshe.com/reaction/25591
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | HCID 178471546 | HCID 178471546 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178486042 | HCID 178486042 | 73% |
Reaction Steps
A solution of 6 g (19.26 mmol) trans-3-[4-(tert-Butoxy carbonyl methyl-amino)-cyclohexyl]-acrylic acid ethyl-ester and 600 mg of Pd/C (10%) was stirred over H2-atmosphere for 20 h. After filtration of the solution, the methanol was evaporated under reduced pressure to yield 5.82 g of clean trans-3-[4-(tert-Butoxycarbonyl methyl-amino)cyclohexyl]-propanoic acid ethyl-ester. To a solution of this ester in 60 ml of THF was added 917 mg (40 mmol) LiBH4. The solution was refluxed for 8 h and then cooled with an ice-bath to 0° C. At this temperature was dropped slowly 1N HCl to the reaction-mixture to destroy excess of LiBH4. The reaction-mixture was diluted with Et2O and then washed with water. The organic layers were evaporated to dryness to yield 3.39 g (73%) of clean trans-[4-(3-Hydroxy-propyl)-cyclohexyl]-methyl-carbamic acid tert-butyl ester, MS: 271 (M).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06858651B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-5b4ca01325a541cfb064a354791af53a |
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| Source note | uspto-grants-2005_02 |
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