HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246920Generated: October 31, 2026
Benzyl chloroformate → Benzyl 3-(hydroxymethyl)azepane-1-carboxylate
https://huagongshe.com/reaction/1246920
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (Azepan-3-yl)methanol | HCID 21901984 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | Benzyl 3-(hydroxymethyl)azepane-1-carboxylate | HCID 20598086 | 94% |
Reaction Steps
Potassium carbonate was added to a mixture of azepan-3-yl-methanol (145) (0.032 g, 0.2485 mmol) in THF/H2O (2:1, 0.31 mL). The suspension was cooled to 0° C., and (benzyloxy)carbonyl chloride (0.071 mL, 0.497 mmol) was added dropwise. The reaction was allowed to warm to room temperature overnight, and was then concentrated in vacuo. CH2Cl2 and H2O were added. The organics were extracted, washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The crude material was purified by automated silica gel chromatography with 75:25 Hexanes:EtOAc to obtain 3-Hydroxymethyl-azepan-1-carboxylic acid benzyl ester (146) in approximately 94% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07129228B2 |
|---|
| Source dataset | uspto-grants-2006_10 |
|---|
| ORD ID | ord-71500117350e40bf885c8952e0a52074 |
|---|
| Source note | uspto-grants-2006_10 |
|---|