HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118231Generated: October 30, 2026
Hydrochloric Acid → HCID 178485999, compound
https://huagongshe.com/reaction/2118231
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Reactant | HCID 178485998 | HCID 178485998 | — |
| Catalyst | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178485999 | HCID 178485999 | 99.4% |
Reaction Steps
To a suspension of 15.0 g (57 mmol) of trans-(4-hydroxy-cyclohexyl)-methyl-carbamic acid benzyl ester in 230 mL of toluene were added 16.8 mL (114 mmol, 2 eq) of bromo-acetic acid tert-butyl ester and 1.93 g (5.7 mmol, 0.1 eq) of tetra-n-butylammonium hydrogensulfate and 400 mL of 50% aqueous NaOH. The mixture was stirred at RT for 4 h, additional 1.93 g (5.7 mmol, 0.1 eq) of tetra-n-butyl-ammoniumhydrogensulfate and 4.2 mL of bromo-acetic acid tert-butyl ester were added, and stirring was continued over night. The solution was concentated and acidified by adding 400 mL of 37% HCl. The solution was extracted with EtOAc, the organic phase was washed with brine and dried over Na2SO4. The solvent was removed to yield 18.2 g (quantitative) trans-[4-(benzyloxycarbonyl-methyl-amino)-cyclohexyloxy]-acetic acid as white solid, MS: 320 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07442791B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-a1fe029bb9e44818b2bf519e300b46a7 |
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| Source note | uspto-grants-2008_10 |
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