HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710439Generated: October 30, 2026
Gabapentin → 1-[[[(1-Chlorobutoxy)carbonyl]amino]methyl]cyclohexaneacetic acid
https://huagongshe.com/reaction/1710439
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Gabapentin | HCID 3446 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 21950270 | HCID 21950270 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[[[(1-Chlorobutoxy)carbonyl]amino]methyl]cyclohexaneacetic acid | HCID 10425219 | 62.1% |
Reaction Steps
To a suspension of gabapentin (8.55 g, 50 mmol) in dichloromethane at 0° C. was added triethylamine (21 mL, 150 mmol) and TMSCl (6.4 mL, 50 mmol). The resulting suspension was stirred at 0° C. for 20 minutes and then a solution of chloroformate (132) (8.55 g, 50 mmol) in dichloromethane was added. The reaction was stirred for another hour at room temperature, then quenched with citric acid and extracted with dichloromethane. The combined organic phase was washed with water and brine and dried over Na2SO4. Filtration and evaporation gave 9.5 g of crude product (133), which was used directly in the subsequent step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07790708B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-07977f5111204d9ab7dcc7b38a6735b8 |
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| Source note | uspto-grants-2010_09 |
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