HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37774Generated: October 27, 2026
Benzyl Alcohol → HCID 67440277, compound
https://huagongshe.com/reaction/37774
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | s-Allylglycine | HCID 167529 | — |
| Product | HCID 67440277 | HCID 67440277 | 68% |
Reaction Steps
To a solution of (2S)-2-amino-4-pentenoic acid 17 (225 mg, 1.96 mmol) in benzyl alcohol (5 mL) was added thionyl chloride (2 mL) and the resulting mixture was allowed to stir for 16 h before addition of diethyl ether (30 mL) and extraction with water (3×30 mL). The aqueous layer was concentrated, diluted with 2M sodium bicarbonate (20 mL), and extracted with DCM (3×30 mL). The combined organic fractions were dried and acidified with 1M HCl/diethyl ether (2 mL) and evaporated. The crude product dissolved in a minimal volume of MeOH and precipitated with diethyl ether to yield the title compound (322 mg, 1.34 mmol, 68%) as a white solid. [α]D20−40.6 (c. 0.1, H2O). Mp 186-191° C. 1H NMR (D2O, 300 MHz): δ 7.28 (m, 5H, ArH); 5.51 (m, 1H, H4); 5.11 (m, 4H, H5 and ArCH2); 4.08 (t, J=5.4 Hz, 1H, H2); 2.55 (m, 2H, H3). Mass Spectrum (CI, +ve) m/z 205 (25%) [MH+]. HRMS calcd for C12H16NO2 206.1181, found 206.1169.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524657B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-373c48794d8c49e3af0729114e0e647c |
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| Source note | uspto-grants-2013_09 |
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