HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2428173Generated: October 31, 2026
2,2,2-Trichloro-tert-butyl chloroformate → (rac.)-(1R*,5S*)-7-[4-(tert-Butyl-dimethyl-silanyloxy)-phenyl]-3,9-diaza-bicyclo[3.3.1]non-6-ene-3,6,9-tricarboxylic Acid 3-tert-butyl Ester 6-ethyl Ester 9-(2,2,2-trichloro-1,1-dimethyl-ethyl) Ester
https://huagongshe.com/reaction/2428173
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,2,2-Trichloro-tert-butyl chloroformate | HCID 5106606 | — |
| Reactant | (rac.)-(1R*,5S*)-7-[4-(tert-Butyl-dimethyl-silanyloxy)-phenyl]-9-methyl-3,9-diaza-bicyclo[3.3.1]non-7-ene-3,6-dicarboxylic Acid 3-tert-butyl Ester 6-ethyl Ester | HCID 131728968 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | (rac.)-(1R*,5S*)-7-[4-(tert-Butyl-dimethyl-silanyloxy)-phenyl]-3,9-diaza-bicyclo[3.3.1]non-6-ene-3,6,9-tricarboxylic Acid 3-tert-butyl Ester 6-ethyl Ester 9-(2,2,2-trichloro-1,1-dimethyl-ethyl) Ester | HCID 131728969 | 90.2% |
Reaction Steps
A mixture of compound B9 (6.16 g, 11.9 mmol) and 2,2,2-trichloro-1,1-dimethylethyl chloroformate (3.15 g, 13.1 mmol) in 1,2-dichloroethane (200 mL) was heated to 60° C. for 20 h. The mixture was allowed to cool to rt, and the solvents were removed under reduced pressure. Purification of the residue by FC (EtOAc/heptane 8:2) yielded the title compound (7.58 g, 90%). LC-MS: tR=1.29 min, ES+: 707.36.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07968720B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-d3aef1d984244af2a5b47a8586fecde5 |
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| Source note | uspto-grants-2011_06 |
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