HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623981Generated: October 30, 2026
Formic Acid → 2-Azatricyclo[3.3.1.13,7]decane-5-carboxylic acid, methyl ester
https://huagongshe.com/reaction/623981
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Fuming sulfuric acid | HCID 24681 | — |
| Reactant | HCID 89720338 | HCID 89720338 | — |
| Product | 2-Azatricyclo[3.3.1.13,7]decane-5-carboxylic acid, methyl ester | HCID 74891108 | 50% |
Reaction Steps
To 2-azatricyclo[3.3.1.13,7]decan-5-ol (Intermediate-7) (1.5 g, 5.9 mmol, 1 eq), 98% formic acid (9 ml) was added drop wise with vigorous gas evolution for over 30 minutes to a rapidly stirred 30% oleum (36 ml) heated to 60° C. Upon completion of this addition, 99% formic acid (9 ml) was slowly added for the next 30 minutes. The reaction mixture was stirred for another 1 hr at 60° C. (monitored by LCMS). The reaction mixture thus formed was then slowly poured into vigorously stirred methanol (75 ml) cooled to 00° C. The mixture was allowed to slowly warm to room temperature while stirring the reaction mixture for 4-5 hrs. The mixture was then concentrated under vacuum. The residue was poured into ice (30 g) and basified with saturated Na2CO3 solution. The aqueous layer was extracted with 5% methanol in DCM (3×100 ml). Combined organic layer was washed with brine and dried over Na2SO4. The organic layer was finally concentrated to get intermediate-8, (550 mg, 50% yield) as an oily mass.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09303016B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-25e8b92db2bc4bee8b57c1a676c36855 |
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| Source note | uspto-grants-2016_04 |
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