HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116031Generated: November 2, 2026
Benzyl chloroformate → HCID 86599133, compound
https://huagongshe.com/reaction/2116031
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 11960770 | HCID 11960770 | — |
| Product | HCID 86599133 | HCID 86599133 | 94% |
Reaction Steps
Treatment of (±)-1-[7-(3-fluorophenyl)-2,3-dihydro-1-benzofuran-2-yl]methanamine (798 g, 6.382.86 mmol) with diisopropylethylamine (0.554 g, 4.29 mmol) followed by benzyl chloroformate (0.536 g, 3.14 mmol) generally according to the procedure described for Intermediate 12 provided 1.01 g (94%) of (±)-benzyl {[7-(3-fluorophenyl)-2,3-dihydro-1-benzofuran-2-yl]methyl}carbamate as a white solid. Rf=0.41 (silica, ethyl acetate:hexanes 2:8); Anal. calcd. for C23H20FNO3: C, 73.2; H, 5.34; N, 3.71. Found: C, 72.96H, 5.38; N, 3.59. Chiral HPLC separation of (±)-benzyl {[7-(3-fluorophenyl)-2,3-dihydro-1-benzofuran-2-yl]methyl}carbamate (Chiralpak OD, isopropanol:hexane 2:8) provided two fractions. Fraction 1 (Rt=7.675 min, Chiralpak OD, isopropanol:hexane 2:8); Fraction 2 (Rt=9.182 min, Chiralpak OD, isopropanol:hexane 2:8).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07435837B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-5f50dbe4720d4f05b762a8b1dd140b19 |
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| Source note | uspto-grants-2008_10 |
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