HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968875Generated: October 29, 2026
Dimethyl Sulfoxide → (4-Formyltetrahydropyran-4-yl)carbamic acid tert-butyl ester
https://huagongshe.com/reaction/1968875
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | tert-butyl N-[4-(hydroxymethyl)oxan-4-yl]carbamate | HCID 67114425 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (4-Formyltetrahydropyran-4-yl)carbamic acid tert-butyl ester | HCID 59718793 | 92.6% |
Reaction Steps
Anhydrous dimethyl sulfoxide (3.0 mL, 42.2 mmol) was added to a −65° C. solution of oxalyl chloride (2.0 mL, 22.9 mmol) in anhydrous dichloromethane (100 mL) and allowed to stir at −65° C. under N2 blanket for 3 minutes, after which time a solution of (4-hydroxymethyl-tetrahydro-pyran-4-yl)-carbamic acid tert-butyl ester (4.89 g, 21.1 mmol) in anhydrous dichloromethane (25 mL) was added. When 25 minutes had elapsed, triethylamine (14.7 mL, 105.5 mmol) was added and the reaction solution allowed to stir for a further 20 minutes at −65° C.; then the cold bath was removed and the reaction warmed to ambient temperature, washed with saturated aqueous sodium chloride (500 mL), dried (MgSO4), and evaporated to afford 4.48 g of clear yellow viscous liquid which was used without further purification. LRMS (ESI) m/z 230.2 [(M+H)+, calcd for C11H20NO4230.3].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08426414B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-1d7bfe9c73174aaabb4bedb2747d1029 |
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| Source note | uspto-grants-2013_04 |
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